TERASON T3000 ULTRASOUND SYSTEMS WITH UPDATED NEEDLE GUIDANCE GRAPHICS
Applicant
Teratech Corp.
Product Code
IYN · Radiology
Decision Date
Feb 3, 2012
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 892.1550
Device Class
Class 2
Attributes
Pediatric, 3rd-Party Reviewed
Indications for Use
The Teratech Corporation Terason t3000™ is a general purpose Ultrasound System intended for use by a qualified physician for evaluation by ultrasound imaging or fluid flow analysis of the human body. Specific clinical applications and exam types include: Fetal, Abdominal, Intra-operative (abdominal, thoracic and PV); Pediatrics, Small Organ (Breast, testes, thyroid); Neonatal and Adult Cephalic; Trans-rectal and Trans-vaginal; Musculo-skeletal (Conventional and Superficial); Cardiac (Adult & Pediatric); Peripheral Vascular.
Device Story
Terason t3000 is a laptop-based diagnostic ultrasound system; utilizes custom engine attached to laptop for acoustic array control and echo processing. New features include six additional transducers and integrated needle guidance technology (10V5S transducer). Needle guidance uses Hall Effect sensors in transducer to track magnet-tipped needle; system generates real-time graphic overlay of needle tip position on ultrasound image. Used by physicians in clinical settings to facilitate accurate needle placement; reduces multiple insertions, trauma, and infection risk. System provides real-time visual feedback to assist clinical decision-making during interventional procedures.
Clinical Evidence
Bench testing only. Compliance with IEC 60601-1, IEC 60601-1-1, IEC 60601-1-4, and IEC 60601-2-37 verified for all new transducers. Biocompatibility testing performed per ISO 10993 Parts 5 and 10. NEMA UD 3 acoustic output display standards met.
Technological Characteristics
Laptop-based system running Windows; custom engine for acoustic array control/processing. Six new transducers added. 10V5S transducer features integrated Hall Effect sensor array for needle tracking. Connectivity via standard laptop interfaces. Sterilization: transducers are patient-contact devices requiring appropriate cleaning/disinfection per user guide. Software-based needle guidance overlay.
Indications for Use
Indicated for diagnostic ultrasound imaging or fluid flow analysis in fetal, abdominal, intra-operative, pediatric, small organ, neonatal/adult cephalic, trans-rectal, trans-vaginal, musculo-skeletal, cardiac, and peripheral vascular applications. Includes ultrasound guidance for needles and catheters.
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.
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K112953
## 510(k) Summary
# FEB - 3 2012
## Teratech Corporation
# Terason t3000™ Ultrasound System
## 1. Sponsor:
Teratech Corporation 77-79 Terrace Hall Ave. Burlington, MA 01803
Contact Person: Ben Chiampa Director of Quality Assurance Telephone: 781-270-4143
Date Prepared: August 15, 2011
Date Modified February 1, 2012
### 2. Device Name
Proprietary Name: Terason t3000 Ultrasound System Common / Usual Name: Diagnostic Ultrasound System Classification Name: Diagnostic Ultrasound Transducer
(21 CFR 892.1570, 90-ITX) Ultrasonic Pulsed Echo Imaging System (21 CFR 892.1560, 90-IYO) Diagnostic Ultrasonic Transducer (21 CFR 892.1570, 90-ITX)
## 3. Predicate Device
Terason™ Echo/t3000 Ultrasound System (K080234)
### 4. Intended Use
The Teratech Corporation Terason t3000™ is a general purpose Ultrasound System intended for use by a qualified physician for evaluation by ultrasound imaging or fluid flow analysis of the human body. Specific clinical applications and exam types include: Fetal, Abdominal, Intra-operative (abdominal, thoracic and PV); Pediatrics, Small Organ (Breast, testes, thyroid); Neonatal and Adult
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Cephalic; Trans-rectal and Trans-vaginal; Musculo-skeletal (Conventional and Superficial); Cardiac (Adult & Pediatric); Peripheral Vascular.
# 5. Device Description
The Terason t3000 is a modified version of the Echo/t3000 Ultrasound System. The modifications include the addition of 6 new transducers (12L5A, 4V2A, 12HL7, 8EC4A, 8EC4V, and 10V5S) and improved needle guidance technology components developed by SOMA Access Systems LLC and integrated into the Terason 10V5S transducer.
# 6. Technology Characteristics
The design and construction of the Terason t3000 is similar to the Terason™ Echo/t3000 Ultrasound system. These systems utilize a laptop computer running Windows to run the ultrasound application and a custom designed engine for control of the acoustic array and processing of the return echoes. The engine is housed in a compartment that is attached to the bottom of the laptop.
The differences between the Terason t3000 and the Terason Echo/t3000 Ultrasound System (the predicate device) include the following:
- Six new transducers have been added to the system. The software has . been modified to control these transducers and ensure compliance to the standards controlling acoustic and thermal power.
- An improved needle guidance technology is provided with the 10V5S . transducer. An array of Hall Effect sensors with a data capture board is integrated into the body of the 10V5S transducer. The sensors track the position of the needle by sensing and determining the position of a magnet located on the needle. This information is transferred through the Terason engine to the application software that generates a graphic overlay upon the ultrasound image showing the position of the tip of the needle to the ultrasound acquired target. The needle tip is a virtual highlight, providing the user with a real time position update, making it easier to insert the needle in the intended target in the first attempt. This improvement is intended to result in significant reductions of multiple insertions, adjustments of needle position during insertions and resultant trauma. infections and ancillary complications from less adequate methods of needle guidance. The needle guidance software component that produces the graphic overlay of needle position is developed by Soma Access
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Systems LLC of Greenville, S.C. and integrated into the Terason t3000 ultrasound software application.
# B1. Non Clinical Tests
The Terason t3000 system has been tested for compliance to the following standards (with the corresponding report referenced for each standard).
- IEC 60601-1 Medical Electrical Equipment Part 1: General . Requirements for Safety.
- o Intertek Test Record Number 3157933BOX-001A
- IEC 60601-1-1, Medical Electrical Equipment Part 1: General . Requirements for Safety Collateral Standard: Safety Requirements for Medical Electrical Systems.
- o Intertek Project: 9157933BOX-001B
- IEC60601-1-4 (2000), Collateral Standard: Safety Requirements for . Medical Electrical Systems
- o Intertek Project: 9157933BOX-001C
- IEC 60601-2-37 / EN60601-2-37 Medical Electrical Equipment Part 2: . Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment.
- Transducer Model 12L5A: Intertek Report Number o 9157933BOX-001E
- o Transducer Model 12HL7: Intertek Report Number 9157933BOX-001F
- o Transducer Model 4V2A: Intertek Report Number 9157933BOX-001N
- o Transducer Model 8EC4A: Intertek Report Number 9157933BOX-001L
- o Transducer Model 8EC4V: Intertek Report Number 3157933BOX-001K
- Transducer Model 10V5S: Intertek Report Number 9157933BOX-001S
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- NEMA UD 3 Acoustic Output Display . Terason t3000/Echo Ultrasound System User Guide (16-3031-15)
- . Biocompatibility Tests, ISO 10993 Part 5 and Part 10
- o Biocompatibility reports for the six new transducers included in this submission.
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Image /page/4/Picture/1 description: The image shows the seal of the U.S. Department of Health and Human Services. The seal is circular and contains the department's emblem in the center. The emblem consists of a stylized caduceus, a symbol of medicine, with a double helix representing DNA. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged around the emblem.
Food and Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993
TERATECH Corporation % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street NW BUFFALO MN 55313
FEB - 3 2012
Re: K112953
Trade/Device Name: Terason t3000 Ultrasound System with updated Needle Guidance Graphics Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: January 20, 2012 Received: January 23, 2012
Dear Mr. Job:
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 Terason t3000 Ultrasound System with updated Needle Guidance Graphics, as described in your premarket notification:
### Transducer Model Number
| 4V2A | 8EC4A | 10V5S |
|------|-------|-------|
| 5C2A | 8EC4V | 12L5A |
| 7L3V | 8MC3 | 12HL7 |
| 8BP4 | 10V5 | 12L5V |
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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 895. 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 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
If you have any questions regarding the content of this letter, please contact Camille Vidal at (301) 796-2645.
Sincerely Yours,
Mary Slater
Mary S. Pastel. Sc.D. Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health
Enclosure(s)
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# Indications for Use Form
510(k) Number (if known): K112953
Device Name: Terason t3000 Ultrasound System with updated Needle Guidance Graphics
Indications for Use:
The subject-modified device is a general purpose Ultrasound System intended for use by a qualified physician for the evaluation by ultrasound imaging or fluid-flow analysis of the human body. Specific clinical applications and exam types include: Fetal, Abdominal, Intra-Operative (spec. and Neuro), Laparoscopic, Pediatric, Small Organ (breast, testes, thyroid), Neonatal and Adult Cephalic, Trans-rectal, Trans-vaginal, Musculo-sketetal (Conventional and Superficial), Cardiac (adult and pediatric), and Peripheral Vascular.
Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
Concurrence of CDRH, Office on In Vitro Diagnostic Devices (OIVD)
Mary S. Pastel.
Division Sign Off Office of In Vitro Diagnostic Device Evaluation 510(k)
Page 1 of 1
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Transducer: (see comments)
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | Otherc |
|-----------------------------|--------------------------------------------------|-------------------|------|------|------|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | |
| Ophthalmic | Ophthalmic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Fetaln | P1,4 | P2,4 | P2,4 | | P2,4 | P2,4 | P2,4 |
| | Abdominald: | P1,4 | P2,4 | P2,4 | P7 | P2,4 | P2,4 | P2,4 |
| | Intra-operative (Spec.)d,e | P4,8 | P4,8 | P4,8 | | P4,8 | P4,8 | P4,8 |
| | Intra-operative (Neuro) | P5 | P5 | P5 | | P5 | P5 | P5 |
| | Laparoscopic | P6 | P6 | P6 | | P6 | P6 | P6 |
| | Pediatricd: | P1,4 | P2,4 | P2,4 | P7 | P2,4 | P2,4 | P2,4 |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | P2,4 | P2,4 | P2,4 | | P2,4 | P2,4 | P2,4 |
| | Neonatal Cephalicd: | P1,4 | P2,4 | P2,4 | P7 | P2,4 | P2,4 | P2,4 |
| | Adult Cephalicd: | P1,4 | P2,4 | P2,4 | P7 | P2,4 | P2,4 | P2,4 |
| | Trans-rectalf: | P2-4 | P3-4 | P3-4 | | P3-4 | P3-4 | P3-4 |
| | Trans-vaginalg: | P2-4 | P3-4 | P3-4 | | P3-4 | P3-4 | P3-4 |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | P2,4 | P2,4 | P2,4 | | P2,4 | P2,4 | P2,4 |
| | Musculo-skel. (Superfic)d: | P2,4 | P2,4 | P2,4 | | P2,4 | P2,4 | P2,4 |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | P1,8 | P2,8 | P2,8 | P7,8 | P2,8 | P2,8 | P2,8 |
| | Cardiac Pediatric | P1,8 | P2,8 | P2,8 | P7,8 | P2,8 | P2,8 | P2,8 |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | P1,4 | P2,4 | P2,4 | | P2,4 | P2,4 | P2,4 |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA (incl. K080234); E= added under Appendix E
1 now multions of Child Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
6 B+M; B+PWD; B+CD; B+DPD; B+PD
6 Harmonic Imaging (HI)
d Incl. ultrasound guidance for placement of needles, catheters
& Abdominal organs and peripheral vessel.
f Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy
9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
1 Incl. stress echo.
1 System uses previously cleared under K992505 with 3MHz Model L3 (Linear)
2 System uses previously cleared under K012191
3 System uses previously cleared under K010883
4 System uses previously cleared under K030191
5 System uses previously cleared under K040840
6 System uses previously cleared under K043278
7 System uses previously cleared under K051334
8 System uses previously cleared under K080234
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Concurrence
Mary Scott
Division Sign-Off
Division Sign Off Office of in Vitro Diagnostic Device ﺮﻛﺔ ﺍﻟﻤ
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### Terason t3000 Ultrasound System_______________________________________________________________________________________________________________________________________________ System:
Transducer: 4V2A
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetald | N | N | N | | N | N | N |
| | Abdominald: | N | N | N | | N | N | N |
| | Intra-operative (Spec.)d,e | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Pediatricd: | N | N | N | | N | N | N |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | | | | | | | |
| | Neonatal Cephalicd: | N | N | N | | N | N | N |
| | Adult Cephalicd: | N | N | N | | N | N | N |
| | Trans-rectalf: | | | | | | | |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | |
| | Musculo-skel. (Superfic)d: | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | N | N | N | | N | N | N |
| | Cardiac Pediatric | N | N | N | | N | N | N |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | | | | | | | |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
N= new nalcation, r = previously cleared by Brit, = (DPD), and (non-directional) Power Dopp. (PD).
6 B+M; B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
4 Incl. ultrasound guidance for placement of needles, catheters
e Abdominal organs and peripheral vessel.
Aboutinal organs and peripherar rooss.
Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy
Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
10 Incl. guidance of amniocentesis, infertility monitoring of follicle development.
1 Incl. stress echo.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S Patil
Office of In Vitro Diagnostic Device Evaluatic 510(k)
Page 1 of _
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Transducer: ' 5C2A
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | | | | | | | |
|-----------------------------|--------------------------------------------------|---|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetaln | E | E | E | | E | E | E |
| | Abdominald: | E | E | E | | E | E | E |
| | Intra-operative (Spec.)d,e | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Pediatricc: | E | E | E | | E | E | E |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | | | | | | | |
| | Neonatal Cephalicd: | | | | | | | |
| | Adult Cephalicd: | | | | | | | |
| | Trans-rectalf: | | | | | | | |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | |
| | Musculo-skel. (Superfic)d: | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | E | E | E | | E | E | E |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
1 Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
0 B+M; B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
9 Incl. ultrasound guidance for placement of needles, catheters
· ª Abdominal organs and peripheral vessel.
' Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy 9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo. .
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S. Poole
Division Sign-Off Office of In Vitro Diagnostic Device FV2 112
Evaluation) and Safety
510(k) K112953
{10}------------------------------------------------
7L3V Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|--|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| | Fetaln | | | | | | | | |
| | Abdominald: | E | E | E | | E | E | E | |
| | Intra-operative (Spec.)d,e | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| Fetal<br>Imaging<br>& Other | Pediatricd: | E | E | E | | E | E | E | |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | E | E | E | | E | E | E | |
| | Neonatal Cephalicd: | E | E | E | | E | E | E | |
| | Adult Cephalicd: | E | E | E | | E | E | E | |
| | Trans-rectalf: | | | | | | | | |
| | Trans-vaginalg: | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skel. (Convent.)d: | E | E | E | | E | E | E | |
| | Musculo-skel. (Superfic)d: | E | E | E | | E | E | E | |
| | Intra-luminal | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| | Cardiac Adult | | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| | | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | E | E | E | | E | E | E | |
| | Other (Specify) | | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
No new libration;
b +M; B+PWD; B+CD; B+DPD; B+PD
6 Harmonic Imaging (HI)
d Incl. ultrasound guidance for placement of needles, catheters
ª Abdominal organs and peripheral vessel.
" Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy
This. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
| Incl. stress echo.
Prescription Use (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S. Pastit
itro Diagnostic Device Fvaluatio
{11}------------------------------------------------
Transducer: 8BP4
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetaln | | | | | | | |
| | Abdominald: | | | | | | | |
| | Intra-operative (Spec.)d,e: | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Pediatricd: | | | | | | | |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | | | | | | | |
| | Neonatal Cephalicd: | | | | | | | |
| | Adult Cephalicd: | | | | | | | |
| | Trans-rectalf: | E | E | E | | E | E | E |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | |
| | Musculo-skel. (Superfic)g: | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | | | | | | | |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
4 Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
b B+M; B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
d Incl. ultrasound guidance for placement of needles, catheters
° Abdominal organs and peripheral vessel.
1 Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy
9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
11 Incl. quidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo.
Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S Pastil
Division Sign-Office of In Vitro Diagnostic Device Evaluation and
{12}------------------------------------------------
8EC4A Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Fetaln | N | N | N | | N | N | N |
| | Abdominald: | | | | | | | |
| | Intra-operative (Spec.)d,e | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatricc: | | | | | | | |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | | | | | | | |
| | Neonatal Cephalicc: | | | | | | | |
| | Adult Cephalicd: | | | | | | | |
| | Trans-rectalf: | N | N | N | | N | N | N |
| | Trans-vaginalg: | N | N | N | | N | N | N |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | |
| | Musculo-skel. (Superfic)d: | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | | | | | | | |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
N - new maloution, i - providered Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
6 B+M; B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
9 Incl. ultrasound guidance for placement of needles, catheters
° Abdominal organs and peripheral vessel.
" Abdominal organs and penpherement of needles, catheters, cryosurgery, and brachytherapy
110. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
Incl. guidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S. Patil
Division Sign-Office of In Vitro Diagnostic Device Evaluati 510(k)
{13}------------------------------------------------
#### System: Terason t3000 Ultrasound System
Transducer: 8EC4V
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|---|-------------------|-----|-----|----------------|-----------------|--------|--|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal<br>Imaging<br>& Other | Fetalh | N | N | N | | N | N | N | |
| | Abdominald: | | | | | | | | |
| | Intra-operative (Spec.)d,a | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatricc: | | | | | | | | |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | | | | | | | | |
| | Neonatal Cephalicc: | | | | | | | | |
| | Adult Cephalicc: | | | | | | | | |
| | Trans-rectalf: | N | N | N | | N | N | N | |
| | Trans-vaginalg: | N | N | N | | N | N | N | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | | |
| | Musculo-skel. (Superfic)d: | | | | | | | | |
| | Intra-luminal | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| | Cardiac Adult | | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | | | | | | | | |
| | Other (Specify) | | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
යි Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
b B+M; B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
d incl. ultrasound guidance for placement of needles, catheters
ీ Abdominal organs and peripheral vessel.
' Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy 9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo.
Prescription Use × (Part 21 CFR 801 Subpart D)
AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary Patel
Division Sigh-Off Office of In Vitro Diagnostic Device Evaluation 510(k) of
Page 1
{14}------------------------------------------------
8MC3 Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
|-----------------------------|--------------------------------------------------|-------------------|---|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | | | | | | | | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| | Fetalh | E | E | E | | E | E | E | |
| Fetal<br>Imaging<br>& Other | Abdominald: | | | | | | | | |
| | Intra-operative (Spec.)d,e | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatricd: | E | E | E | | E | E | E | |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | E | E | E | | E | E | E | |
| | Neonatal Cephalicd: | E | E | E | | E | E | E | |
| | Adult Cephalicd: | E | E | E | | E | E | E | |
| | Trans-rectalf: | | | | | | | | |
| | Trans-vaginalg: | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | | |
| | Musculo-skel. (Superfic)d: | | | | | | | | |
| | Intra-luminal | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Cardiac | Cardiac Adult | E | E | E | | E | E | E | |
| | Cardiac Pediatric | E | E | E | | E | E | E | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | E | E | E | | E | E | E | |
| | Other (Specify) | | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
Now Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
0 B+M: B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
d Incl. ultrasound guidance for placement of needles, catheters
e Abdominal organs and peripheral vessel.
" Abouthinal organs and perfibrarrent of needles, catheters, cryosurgery, and brachytherapy
9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
10 Incl. guidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S. Postel
Division Sign-Off Office of In Vitro Diagnostic Device Evaluatic 510(k)
{15}------------------------------------------------
#### System: Terason t3000 Ultrasound System
Transducer: 10V5
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetaln | | | | | | | |
| | Abdominald: | | | | | | | |
| | Intra-operative (Spec.)d,e) | P | P | P | | P | P | P |
| | Intra-operative (Neuro) | P | P | P | | P | P | P |
| | Laparoscopic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Pediatricc: | P | P | P | | P | P | P |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | P | P | P | | P | P | P |
| | Neonatal Cephalicc: | P | P | P | | P | P | P |
| | Adult Cephalicc: | P | P | P | | P | P | P |
| | Trans-rectalf: | | | | | | | |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | | | | | | | |
| | Musculo-skel. (Superfic)d: | | | | | | | |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | P | P | P | | P | P | P |
| | Cardiac Pediatric | P | P | P | | P | P | P |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | | | | | | | |
| | Other (Specify) | | | | | | | |
N= new indication: P= previously cleared by FDA (incl. K040840; E= added under Appendix E
3 Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
b B+M; B+PWD; B+CD; B+DPD; B+PD
6 Harmonic Imaging (HI)
d Incl. ultrasound guidance for placement of needles, catheters
* Abdominal organs and peripheral vessel.
Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy
9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
11 Incl. guidance of amniocentesis, infertility monitoring of follicle development.
Incl. stress echo.
1 System uses previously cleared under K040840
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S Pastil
isinn Sian fice of In Vitro Diagnostic Device Fraluation and
510(k) K112953
{16}------------------------------------------------
10V5S Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Intended Use: Diagnostic ultrasound imaging of fluid flow analysis of the vascular system | | | | | | | | |
|-------------------------------------------------------------------------------------------|--------------------------------------------------|---|---|-----|-----|----------------|-----------------|--------|
| Clinical Application | Mode of Operation | | | | | | | |
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Fetaln | | | | | | | |
| | Abdominald: | N | N | N | | N | N | |
| | Intra-operative (Spec.)d,e,i | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatricd: | N | N | N | | N | N | |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | N | N | N | | N | N | |
| | Neonatal Cephalicd: | N | N | N | | N | N | |
| | Adult Cephalicd: | N | N | N | | N | N | |
| | Trans-rectalf: | | | | | | | |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | N | N | N | | N | N | |
| | Musculo-skel. (Superfic)d: | N | N | N | | N | N | |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | N | N | N | | N | N | |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
1 Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
b B+M; B+PWD; B+CD; B+DPD; B+PD
6 Harmonic Imaging (HI)
8 Incl. ultrasound guidance for placement of needles, catheters
e Abdominal organs and peripheral vessel.
' / nodominal organe and perpheral vost of needles, catheters, cryosurgery, and brachytherapy
9 Incl. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary Scott
Division Sign-Off Office of In Vitro Diagnostic De Evaluatio
Evaluation and Safety
510(k) K112953
{17}------------------------------------------------
12L5A Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetalh | | | | | | | |
| | Abdominald: | N | N | N | | N | N | N |
| | Intra-operative (Spec.)d,e | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Pediatricd: | N | N | N | | N | N | N |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | N | N | N | | N | N | N |
| | Neonatal Cephalicd: | N | N | N | | N | N | N |
| | Adult Cephalicd: | N | N | N | | N | N | N |
| | Trans-rectalf: | | | | | | | |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | N | N | N | | N | N | N |
| | Musculo-skel. (Superfic)d: | N | N | N | | N | N | N |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral | Peripheral vesseld: | N | N | N | | N | N | N |
| Vessel | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
4 Includes Color Dopp. (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
0 B+M; B+PWD; B+CD; B+DPD; B+PD
6 Harmonic Imaging (HI)
d Incl. ultrasound guidance for placement of needles, catheters
e Abdominal organs and peripheral vessel.
' Incl. ultrasound guidance for placement of needles, catheters, cryosurgery, and brachytherapy
9 Inol. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
' Incl. stress echo.
Prescription Use (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S Patil
Division Sign-Off Office of In Vitro Diagnostic Device Evaluațic 510(k)
Page 1 of
{18}------------------------------------------------
Transducer: 12HL7
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Fetaln | | | | | | | |
| | Abdominald: | | | | | | | |
| | Intra-operative (Spec.)d,e | N | N | N | | N | N | N |
| | Intra-operative (Neuro) | N | N | N | | N | N | N |
| | Laparoscopic | N | N | N | | N | N | N |
| | Pediatricd: | N | N | N | | N | N | N |
| | Small Organ (Thyroid,<br>Breast, Testes, etc.)d: | N | N | N | | N | N | N |
| | Neonatal Cephalicd: | | | | | | | |
| | Adult Cephalicd: | | | | | | | |
| | Trans-rectalf: | | | | | | | |
| | Trans-vaginalg: | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skel. (Convent.)d: | N | N | N | | N | N | N |
| | Musculo-skel. (Superfic)d: | N | N | N | | N | N | N |
| | Intra-luminal | | | | | | | |
| | Other (Specify) | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Other (Specify) | | | | | | | |
| Peripheral<br>Vessel | Peripheral vesseld: | N | N | N | | N | N | N |
| | Other (Specify) | | | | | | | |
N= new indication; P= previously cleared by FDA; E= added under Appendix E
N = new manager, (CD), Directional Power Dopp. (DPD), and (non-directional) Power Dopp. (PD).
8 B+M; B+PWD; B+CD; B+DPD; B+PD
° Harmonic Imaging (HI)
9 Incl. ultrasound guidance for placement of needles, catheters
° Abdominal organs and peripheral vessel.
Aboominal organo and penphora 1800 of needles, catheters, cryosurgery, and brachytherapy
This. ultrasound guidance of transvaginal biopsy, infertility monitoring of follicle development.
" Incl. guidance of amniocentesis, infertility monitoring of follicle development.
Incl. stress echo.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Mary S Patil
Office of In Vitro Evaluation 510(K)
{19}------------------------------------------------
12L5V Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | |
|-----------------------------|--------------------------------------------------|-------------------|---|-----|-----|----------------|-----------------|--------|
| General<br>(Track I Only) | Specific<br>(Tracks I & III) | B | M | PWD | CWD | Color<br>Doppa | Comb.<br>Modesb | Otherc |
| Ophthalmic | Ophthalmic | | | | | | | |
| Fetal<br>Imaging<br>& Other | Fetaln | | | | | | | |
| |…
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.