K063518 · Hitachi Medical Systems America, Inc. · IYN · Dec 21, 2006 · Radiology
Device Facts
Record ID
K063518
Device Name
HI VISION 900 DIAGNOSTIC ULTRASOUND SCANNER
Applicant
Hitachi Medical Systems America, Inc.
Product Code
IYN · Radiology
Decision Date
Dec 21, 2006
Decision
SESE
Submission Type
Special
Regulation
21 CFR 892.1550
Device Class
Class 2
Attributes
Pediatric
Indications for Use
Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:
Device Story
The Hitachi HI VISION 900 is a diagnostic ultrasound system utilizing pulsed echo and pulsed Doppler imaging. It processes acoustic signals from various transducers to generate B-mode, M-mode, Pulsed Wave Doppler, Continuous Wave Doppler, Color Flow, Amplitude Doppler, Harmonic, and 3D images. Operated by clinicians in clinical settings, the system provides real-time visualization of internal structures and blood flow. Output is displayed for the clinician to guide diagnostic assessments, interventional procedures (e.g., biopsies), and surgical planning. The device aids in clinical decision-making by providing non-invasive anatomical and hemodynamic data, potentially improving diagnostic accuracy and procedural safety.
Clinical Evidence
Bench testing only. The device complies with NEMA UD-3 (Standard for Real-Time Display of Thermal and Mechanical Acoustic Output Indices) and the 510(k) Diagnostic Ultrasound Guidance (April 14, 1994). General safety is verified through compliance with IEC 60601-1.
Technological Characteristics
Diagnostic ultrasound system supporting B-mode, M-mode, PWD, CWD, Color Doppler, Amplitude Doppler, Harmonic, and 3D imaging. Complies with NEMA UD-3 and IEC 60601-1. Supports multiple transducer types (e.g., EUP-B514, EUP-F531, EUP-850, EUP-C514, EUP-L53S, EUP-TC3, EUP-C532, EUP-L65, EUP-U533, EUP-CC531, EUP-053T, EUP-V53W, EUP-CV524, EUP-OL334, EUP-ES52M, EUP-R54AW).
Indications for Use
Indicated for diagnostic ultrasound imaging or fluid flow analysis of the human body, including fetal, abdominal, intra-operative, pediatric, small organ, neonatal cephalic, adult cephalic, transrectal, transvaginal, musculoskeletal, cardiac, and peripheral vessel applications. Includes guidance for percutaneous biopsy of abdominal organs, amniocentesis, and surgical procedures (excluding neurosurgery and laparoscopic).
Regulatory Classification
Identification
An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
Submission Summary (Full Text)
{0}------------------------------------------------
# Device Description
The Hitachi HI VISION 900 Diagnostic Ultrasound Scanner is a Track 3 Diagnostic Ultrasound Pulsed Doppler and Pulsed Echo Imaging System capable of the following operating functions:
- . B Mode
- M Mode .
- . Pulsed Wave Doppler
- . Continuous Wave Doppler
- . Color Flow
- . Amplitude Doppler
- Harmonic imaging .
- . Superficial musculoskeletal imaging
- . 3D imaging
# Safety
As a Track 3 ultrasound device, the Hitachi HI VISION 900 Diagnostic Ultrasound Scanner complies with the Standard for Real-Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment (1992) - published by NEMA as UD-3.
With respect to limits on acoustic outputs, the Hitachi HI VISION 900 Diagnostic Ultrasound Scanner complies with the guideline limits set in the 510(k) Diagnostic Ultrasound Guidance - Revision: April 14, 1994.
With regard to general safety, the Hitachi HI VISION 900 Diagnostic Ultrasound Scanner is designed to comply with IEC 606601-1 (1998) Medical Electrical Equipment, Part 1 - General Requirements for Safety.
{1}------------------------------------------------
Image /page/1/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized depiction of an eagle or bird-like figure with three curved lines representing its wings or body. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular fashion around the bird symbol.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
1
DEC 2 1 2006
Mr. Douglas J. Thistlewaite Manager of Regulatory Affairs HITACHI Medical Systems America, Inc. 1959 Summit Commerce Park TWINSBURG OH 44087-2371
Re: K063518
Trade Name: HI VISION 900 Diagnostic Ultrasound Scanner Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulation Number: 21 CFR 892.1570 Regulation Name: Diagnostic ultrasonic transducer Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: November 20, 2006 Received: November 21, 2006
Dear Mr. Thistlewaite:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
This determination of substantial equivalence applies to the following transducers intended for use with the HI VISION 900 Diagnostic Ultrasound Scanner, as described in your premarket notification:
Image /page/1/Picture/11 description: The image shows a circular logo with the letters "FDA" in bold, stylized font at the center. Above the letters, the years "1906-2006" are printed. Below the letters, the word "Centennial" is written in cursive. The logo is surrounded by text that reads "A CENTURY OF SERVICE TO CONSUMER PROTECTION & HEALTH IN THE SCIENCE OF FOODS". The logo appears to be a commemorative emblem, possibly celebrating the 100th anniversary of an organization.
Protecting and Promoting Public Health
{2}------------------------------------------------
#### Transducer Model Number EUP-B514 EUP-F531 EUP-850 EUP-C514 EUP-L53S EUP-TC3 EUP-C532 EUP-L65 EUP-U533 EUP-CC531 EUP-053T EUP-V53W EUP-CV524 EUP-OL334 EUP-ES52M EUP-R54AW-19, -33
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
This determination of substantial equivalence is granted on the condition that prior to shipping the first device, you submit a postclearance special report. This report should contain complete information, including acoustic output measurements based on production line devices, requested in Appendix G, (enclosed) of the Center's September 30, 1997 "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers." If the special report is incomplete or contains unacceptable values (e.g., acoustic output greater than approved levels), then the 510(k) clearance may not apply to the production units which as a result may be considered adulterated or misbranded.
The special report should reference the manufacturer's 510(k) number. It should be clearly and prominently marked "ADD-TO-FILE" and should be submitted in duplicate to:
> Food and Drug Administration Center for Devices and Radiological Health Document Mail Center (HFZ-401) 9200 Corporate Boulevard Rockville, Maryland 20850
This letter will allow you to begin marketing your device as described in your premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus permits your device to proceed to market.
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{3}------------------------------------------------
Page 2 - Mr. Thistlewaite
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html
If you have any questions regarding the content of this letter, please contact Andrew Kang at (240) 276-3666.
Sincerely yours,
David A. Segura
Nancy C. Brogdon Director, Division of Reproductive, Abdominal and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure(s)
{4}------------------------------------------------
### DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE FORM 006 NOTSTA IH
| Clinical Application | | Mode of Operation | | | | | | Other**<br>(Spec.) |
|---------------------------|------------------------------|-------------------|----|-----|-----|------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | |
| Ophthalmic | Ophthalmic | N | N | N | N | N | N | N |
| | Fetal | N | N | N | N | N | N | N |
| | Abdominal | Na | Na | Na | Na | Na | Na | Na |
| | Intra-operative (Spec.) | Nb | Nb | Nb | | Nb | Nb | Nb |
| | Intra operative (Neuro.) | | | | | | | |
| | Laparoscopic | N | N | N | | N | N | N |
| | Pediatric | N | N | N | N | N | N | N |
| | Small Organ (Spec.) | Nd | Nd | Nd | | Nd | Nd | Nd |
| | Neonatal Cephalic | N | N | N | | N | N | N |
| Fotal Imaging<br>& Other | Adult Cephalic | N | N | N | N | N | N | N |
| | Trans rectal | Nh | Nh | Nh | | Nh | Nh | Nh |
| | Trans-vaginal | Nf | Nf | Nf | | Nf | Nf | Nf |
| | Trans-urethral | | | | | | | |
| | Trans esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | N | N | N | | N | N | N |
| | Musculo-skel. (Superfic.) | N | N | N | | N | N | N |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| Cardiac | Cardiac Adult | N | N | N | N | N | N | N |
| | Cardiac Pediatric | N | N | N | N | N | N | N |
| | Trans esophageal (card.) | Ng | Ng | Ng | N | Ng | Ng | Ng |
| | Other (spec.) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | N | N | N | N | N | N | N |
| | Other (spec.) | | | | | | | |
Intended use. Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:
N = new indication, P = previous indication
*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.
** Amplitude Dopplor, Harmonic Imaging and 3D Imaging.
#### Additional Comments:
System:
Includes imaging for guidance of percutaneous biopay of abdominal organs and structures Subscript "a": (including amniocentesis)
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
An a paran A DEBOY
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
David R. Hyman
(Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number ________________________________________________________________________________________________________________________________________________________________
Prescription Use (Per 21 CFR 801.109)
647089808814
BRITEMA SMATEVS lesibeM idaesiH-mori
me 2p : 7 |
{5}------------------------------------------------
System: HI VISION 900
Transducer: EUP-B514
| Clinical Application | | Mode of Operation | | | | | | |
|---------------------------|------------------------------|-------------------|----|-----|-----|------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal | P | P | P | | P | P | P |
| | Abdominal | Pa | Pa | P | | Pa | Pa | Pa |
| | Intra-operative (Spec.) | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | | | | | | | |
| | Small Organ (Spec.) | | | | | | | |
| | Neonatal Cephalic | | | | | | | |
| Fetal Imaging<br>& Other | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | |
| | Musculo-skel. (Superfic.) | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Trans-esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | | | | | | | |
| | Other (spec.) | | | | | | | |
Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human hody as follows
N = new indication, P = previous indication
*Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler and Harmonic Imaging
Additional Comments:
| Subscript "a": | Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures<br>(including amniocentesis). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off) Division of Reproductive, Abdominal, ENT and Radiological Devices
510(k) Number: K063518
David A. Lygum
(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices 510(k) Number _
Prescription Use (Per 21 CFR 801.109)
6720E960868889
ше Zy:Z |
{6}------------------------------------------------
### DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE FORM 06 NOTERS H
System: Transducer:
EUP-C514
| Clinical Application | | Mode of Operation | | | | | | |
|---------------------------|------------------------------|-------------------|----|-----|-----|------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| Fetal Imaging<br>& Other | Fetal | P | P | P | | P | P | P |
| | Abdominal | Pa | Pa | Pa | | Pa | Pa | Pa |
| | Intra-operative (Spec.) | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | P | P |
| | Small Organ (Spec.) | Pd | Pd | Pd | | Pd | Pd | Pd |
| | Neonatal Cephalic | | | | | | | |
| | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | |
| | Musculo-skel. (Superfic.) | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Trans esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | | | | | | | |
| | Other (spec.) | | | | | | | |
#### Intended use. Diagnostic ultragound imaging or fluid flow analysis if the human body as follows
N = new indication, P = previous indication
* Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler, Harmonic Imaging and 3D Imaging,
Additional Comments:
Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures Subscript "a": (including amniocentesis).
| Subscript "b": Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
|------------------------------------------------------------------------------------------------------------------------------------------|
| Subscript "c": Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": For pediatric patients. |
| Subscript "h": Includes imaging for guidance of transrectal biopsy. |
| (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) |
Concurrence of CDRH, Office of Device Evaluation (ODE)
Division Sign-Off Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
(Division Sign-Off)
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K06351
Prescription Use (Per 21 CFR 801,109)
44706880000114
180178mA 2metry2 leaibeM idastin-mori 90-61-200 me2☆:Z}
{7}------------------------------------------------
System -Transduce:
| HI VISION 900 | |
|---------------|--|
| EUP-C532 | |
| Clinical Application | | Mode of Operation | | | | | | |
|---------------------------|------------------------------|-------------------|----|-----|-----|------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal | | | | | | | |
| | Abdominal | Pa | Pa | Pa | | Pa | Pa | Pa |
| | Intra-operative (Spec.) | Pb | Pb | Pb | | Pb | Pb | Pb |
| | Intra-operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | P | P |
| | Small Organ (Spec.) | Pd | Pd | Pd | | Pd | Pd | Pd |
| | Neonatal Cephalic | P | P | P | | P | P | P |
| Fetal Imaging<br>& Other | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | |
| | Musculo-skel. (Superfic.) | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | P | P | P | | P | P | P |
| | Other (spec.) | | | | | | | |
Intended use. Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows
N = new indication, P = previous indication
*Combination of each operating mode, B, M. PWD and Color Doppler.
** Amplitude Doppler and Harmonic Imaging
Additional Comments:
Subscript "Includes imaging for guidance of percutaneous biopoy of abdominal organs and structures
| | (including amniocentesis). |
|----------------|-------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery |
| | (excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
| | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) |
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off) Division of Reproductive, Abdominal, ENT. and Radiological Devices
510(k) Number: K063518
(Division Sign-Off)
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K063518
Prescription Use (Per 21 CFR 801.109)
1997 1977 1991 1991 18 189 1991 1991 19 90-61-200 12:488mm
{8}------------------------------------------------
System Transducer:
006 NOTSION 900 EUP-CC531
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------|----------|----------|-----|------------------|----------------------|--------------------|--|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | FWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging<br>& Other | Fetal<br>Abdominal<br>Intra operative (Spec.)<br>Intra-operative (Neuro.)<br>Laparoscopic<br>Pediatric<br>Small Organ (Spec.)<br>Neonatal Cephalic | P | P | P | | P | P | P | |
| | Adult Cephalic<br>Trans-rectal<br>Trans-vaginal<br>Trans-urethral<br>Trans-esoph. (non-Card.)<br>Musculo-skel. (Convent.)<br>Musculo-skel. (Superfic.) | Pe<br>Pf | Pe<br>Pf | Pe<br>Pf | | Pe<br>Pf | Pe<br>Pf | Pe<br>Pf | |
| | Intra-luminal<br>Other (spec.) | | | | | | | | |
| Cardiac | Cardiac Adult<br>Cardiac Pediatric<br>Trans-esophageal (card.)<br>Other (spec.) | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel<br>Other (spec.) | | | | | | | | |
Intended use: Diagnostic ultrasound inaging or fluid flow analysis if the human body as follows
N = new indication, P = previous indication
*Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler and Harmonic Imaging
Additional Comments:
Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures Subscript "a": (including amniocentesis).
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED (FLEASE DO MO) Concurrence of CDRH, Office of Device Evaluation (ODE)
> (Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
(Division Sign-Off)
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number 2063518
Prescription Use (Per 21 CFR 801.109)
ની
{9}------------------------------------------------
#### DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE FORM 006 NOTSION 900
System: Transducer:
CUP-CV524
| Clinical Application | | Mode of Operation | | | | | | |
|---------------------------|------------------------------|-------------------|---|-----|-----|------------------|---------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal | P | P | P | | P | P | P |
| | Abdominal | P | P | P | | P | P | P |
| | Intra-operative (Spec.) | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | P | P |
| | Small Organ (Spec.) | P | P | P | | P | P | P |
| | Neonatal Cephalic | | | | | | | |
| Fetal Imaging<br>& Other | Adult Cephalic | | | | | | | |
| | Trans rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | |
| | Musculo-skel. (Superfic.) | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | | | | | | | |
| | Other (spec.) | | | | | | | |
Intended use' Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows
N = new indication, P = previous indication
* Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler, Harmonic Imaging and 3D Imaging.
### Additional Comments:
| Subscript "a": | Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures<br>(including amniocentesis). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED PLEASE DO NOT
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
David h. Segram
(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices 510(k) Number ________________________________________________________________________________________________________________________________________________________________
Prescription Use (Per 21 CFR 801.109)
1688-1 020/800 . 9 EBO-T - 677069606800814
so irema smetzy s les ibel interit-mori שפיל : קישורים 90-61-200
{10}------------------------------------------------
Transducer: EUP ES52M
System:
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|------------------------------|-------------------|---|-----|-----|------------------|----------------------|--------------------|--|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| | Fetal | | | | | | | | |
| | Abdominal | | | | | | | | |
| | Intra operative (Spec.) | | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | | | | | | | | |
| | Small Organ (Spec.) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| Fetal Imaging<br>& Other | Adult Cephalic | | | | | | | | |
| | Trans-rectal | | | | | | | | |
| | Trans-vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | | |
| | Musculo-skel. (Superfic.) | | | | | | | | |
| | Intra-luminal | | | | | | | | |
| | Other (spec.) | | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Trans-esophageal (card.) | P | P | P | P | P | P | P | |
| | Other (spec.) | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | | | | | | | | |
| | Other (spec.) | | | | | | | | |
N = new indication, 1' = previous indication
*Combination of each operating mode. B. M. PWD, CWD and Color Doppler.
** Amplitude Doppler
Additional Comments'
Subscript "g" Includes imaging for guidance of percutancous biopsy of abdominal organs and structures
| | (including amniocentesis). |
|----------------|-------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery |
| | (excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
| | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) |
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
David A. Ingram
---
(Division Sign-Off)
Division of Reproductive, Abdomi and Radiological Devices 510(k) Number _
Prescription Use (Per 21 CFR 801, 109)
{11}------------------------------------------------
# DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE FORM 006 NOTSION 900
Transducer: EUP-F531
System -
| | Clinical Application | | | | | Mode of Operation | | |
|---------------------------|------------------------------|----|----|-----|-----|-------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal<br>Abdominal | P | P | P | | P | P | P |
| | Intra-operative (Spec.) | Pb | Pb | Pb | | Pb | Pb | Pb |
| | Intra operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | P | P |
| | Small Organ (Spec.) | Pc | Pc | Pc | | Pc | Pc | Pc |
| | Neonatal Cephalic | P | P | P | | P | P | P |
| Fetal Imaging | Adult Cephalic | | | | | | | |
| & Other | Trans-rectal | P | P | P | | P | P | P |
| | Trans vaginal | P | P | P | | P | P | P |
| | Trans-urethral | | | | | | | |
| | Trans-esoph, (non Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | |
| | Musculo skel. (Superfic.) | | | | | | | |
| | Intra luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Peripheral | Peripheral vessel | P | P | P | | P | P | P |
| Vessel | Other (spec.) | | | | | | | |
Intended use: Diagnostic ultrasound imaging or fluid flow enalysis if the human body as follows:
N = new indication, P = previous indication
* Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler and Harmonic Imaging.
Additional Comments: Stibscript "4": ۲۰۰۵۱۰۰۵
| Subscript "a": | Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures<br>(including amniocentesis). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
S LINE-CONTINUE ON ANOTHER PAGE IF NEEDED ALLE, BALLOW
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number:
David A. Bergmann
KO6351
(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices 510(k) Number .
Prescription Use (Per 21 CFR 801.109)
:
{12}------------------------------------------------
System' Transduce
| HI VISION 900 |
|---------------|
| EUP-L53S |
| | Clinical Application | Mode of Operation | | | | | | |
|---------------------------|------------------------------|-------------------|----|-----|-----|------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| | Ophthalmic | | | | | | | |
| | Fetal | | | | | | | |
| | Abdominal | Pa | Pa | Pa | | Pa | Pa | Pa |
| | Intra-operative (Spec.) | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | P | P |
| Fetal Imaging<br>& Other | Small Organ (Spec.) | Pd | Pd | Pd | | Pd | Pd | Pd |
| | Neonatal Cephalic | | | | | | | |
| | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel (Convent.) | P | P | P | | P | P | P |
| | Musculo-skel. (Superfic.) | P | P | P | | P | P | P |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans-esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Peripheral | Peripheral vessel | P | P | P | | P | P | P |
| Vessel | Other (spec.) | | | | | | | |
Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows
N = new indication, P = previous indication
* Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler, Harmonic Imaging and 3D Imaging,
Additional Comments:
Subscript "A" Includes imaging for guidance of perculaneous biopsy of abdominal organs and structures (including amniocentesis).
| Subscript "b": | Includes imaging of organs and structures exposed during surgery |
|----------------|-------------------------------------------------------------------------------------------|
| | (excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) (PLEASE DO NOT Concurrence of CDRH. Office of Device Evaluation (ODE)
> Division Sign-Off Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
David R. Lehman
(Division Sign-Off) Onliston of Reproductive, Abdom ann Radiological Devices 5114k) Number _
Preseription Use (Per 21 CFR 801.109)
। ୧୫---020/210.9 £80-1 BATOEGROEE I +
soilema smatzy2 feaibeM idastiH-mor7 12:44am 80-61-200
{13}------------------------------------------------
System: Transducer:
# EUP-LG5
| Clinical Application | | Mode of Operation | | | | | | |
|---------------------------|------------------------------|-------------------|----|-----|-----|------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal | | | | | | | |
| | Abdominal | P | P | P | | P | P | P |
| | Intra-operative (Spec.) | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | P | P |
| | Small Organ (Spec.) | Pc | Pc | Pc | | Pc | Pc | Pc |
| | Neonatal Cephalic | | | | | | | |
| Fetal Imaging<br>& Other | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethra) | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.) | P | P | P | | P | P | P |
| | Musculo-skel. (Superfic.) | P | P | P | | P | P | P |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans-esophageal (card.) | | | | | | | |
| | Other (spec.) | | | | | | | |
| | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | P | P | P | | P | P | P |
| | Other (spec.) | | | | | | | |
Intended use. Dirasound imaging or fluid flow analysis if the human body as follows:
N = new indication, P = previous indication
*Combination of each operating mode, B, M, PWD and Color Doppler.
** Amplitude Doppler and Harmonic Imaging.
# Additional Comments:
| Subscript "a": | Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures<br>(including amniocentesis). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
Subscript "g": For pediatric patients. Subscript "h": ipt "h": Includes imaging for guidance of transectal biopay.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEBDED
(PLEASE DO NOT WRITE BELOW THIS LINE. CONTINUED ON ANOTHER PAGE)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Division Sign-Off Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number: K063518
David R. Segmen
---
(Division Sign-Off)
Division of Reproductive, Abdomin and Radiological Devices 510(k) Number ___
Prescription Use (Per 21 CFR 801.109)
Ania Sales Saletses Tesibel infortill-mori
ાજે
{14}------------------------------------------------
System: 006 NOISION 900
Transducer: EUP-0531
| | Clinical Application | | | | | Mode of Operation | | |
|---------------------------|------------------------------------------------------|----|----|-----|-----|-------------------|----------------------|--------------------|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other**<br>(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal<br>Abdominal | | | | | | | |
| Fetal Imaging<br>& Other | Intra-operative (Spec.)<br>Intra-operative (Neuro.) | Pb | Pb | Pb | | Pb | Pb | Pb |
| | Laparoscopic<br>Pediatric | | | | | | | |
| | Small Organ (Spec.)<br>Neonatal Cephalic | | | | | | | |
| | Adult Cephalic<br>Trans-rectal | | | | | | | |
| | Trans-vaginal<br>Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.)<br>Musculo-skel. (Convent.) | | | | | | | |
| | Musculo-skel. (Superfic.)<br>Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| Cardiac | Cardiac Adult<br>Cardiac Pediatric | | | | | | | |
| | Trans-esophageal (card.)<br>Other (spec.) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel<br>Other (spec.) | | | | | | | |
| Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows: | |
|--------------------------------------------------------------------------------------------------|--|
|--------------------------------------------------------------------------------------------------|--|
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
N = new indication, P = previous indication
* Combination of each operating mode, B, M. PWD and Color Doppler.
** Amplitude Doppler and Harmonic Imaging.
#### Additional Comments:
| Subscript "a": | Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures<br>(including amniocentesis). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed during surgery<br>(excluding neurosurgery and laparoscopic procedures). |
| Subscript "c": | Includes thyroid, parathyroid, breast, scrotum, penis. |
| Subscript "d": | Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy. |
| Subscript "e": | Includes imaging for guidance of transrectal biopsy. |
| Subscript "f": | Includes imaging for guidance of transvaginal biopsy. |
| Subscript "g": | For pediatric patients. |
| Subscript "h": | Includes imaging for guidance of transrectal biopsy. |
WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED CLEASE DO NOT Concurrence of CDRH, Office of Device Evaluation (ODE)
> (Division Sign-Off) Division of Reproductive, Abdominal, ENT and Radiological Devices
510(k) Number: K063518
David Ch. Lyonn
(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices 510(k) Number _
Prescription Use (Per 21 CFR 801.109)
| 88-3 020/410.9 180-1 647069808814
so inema smetzy si system idae substil-mori
14
Dac-18-06
12:44am
{15}------------------------------------------------
# DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE FORM 006 NOTSION 900
System: Transducer: EUP-OL334
| | Clinical Application | | | | | | Mode of Operation | | | |
|---------------------------|------------------------------|---|---|-----|-----|------------------|----------------------|---------------------|--|--|
| General<br>(Track I only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppler | Combined*<br>(Spec.) | Other **<br>(Spec.) | | |
| Ophthalmic | Ophthalmic | | | | | | | | | |
| | Fetal | | | | | | | | | |
| | Abdominal | | | | | | | | | |
| | Intra-operative (Spec.) | | | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | | | |
| | Laparoscopic | P | P | P | | P | P | P | | |
| | Pediatric | | | | | | | | | |
| | Small Organ (Spec.) | | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | | |
| Fetal Imaging<br>& Other | Adult Cephalic | | | | | | | | | |
| | Trans-rectal | | | | | | | | | |
| | Trans-vaginal | | | | | | | | | |
| | Trans-urethral | | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | | |
| | Musculo-skel. (Convent.) | | | | | | | | | |
| | Musculo-skel. (Superfic.) | | | | | | | | | |
| | Intra-luminal | | | | | | | | | |
| | Other (spec.) | | | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | | |
| | Trans-esophageal (card.) | | | | | | | | | |
| | Other (spec.) | | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vessel | | | | | | | | | |
| | Other (spec.) | | | | | | | | | |
# Intended use . Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:
N = new indication, P = previous indication
"Combination of each operating mode, B, M, PWD and Color Doppler.
**Amplitude Doppler
Additional Comments:
| Subscript "a": | Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures<br>(including amniocentesis). |
|----------------|---------------------------------------------------------------------------------------------------------------------------|
| Subscript "b": | Includes imaging of organs and structures exposed…
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.