← Product Code [IYO](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO) · K122574
# DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL D3 AND D6 (K122574)
_Edan Instruments, Inc. · IYO · Oct 12, 2012 · Radiology · SESE_
**Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO/K122574
## Device Facts
- **Applicant:** Edan Instruments, Inc.
- **Product Code:** [IYO](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO.md)
- **Decision Date:** Oct 12, 2012
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 892.1560
- **Device Class:** Class 2
- **Review Panel:** Radiology
- **Attributes:** Pediatric, 3rd-Party Reviewed
## Indications for Use
The D3 and D6 Digital Ultrasonic Diagnostic Imaging System are applicable for adult or children ultrasound evaluation in hospitals, clinics, gynecology rooms, obstetrics rooms, examination rooms, intensive care units, and emergency rooms The D3 and D6 are intended for use by or on the order of a physician or similarly qualified health care professional for ultrasound evaluation of Fetus; Abdomen; Pediatrics; Small Organ; Neonatal head; Cardiology; Peripheral Vessel; Musculo-skeleton (both Conventional and Superficial); Urology (including prostate); Transrecta and Transvagina.
## Device Story
Portable digital ultrasonic diagnostic imaging system (Models D3, D6) for clinical diagnostic examination. Device emits ultrasound waves into body tissue via array transducers (linear, convex, microconvex, transrectal, transvaginal; 2.0-10.0 MHz) and processes returned echoes. Displays images in B-Mode, 2B-Mode, 4B-Mode, M-Mode, and B+M Mode. Operated by physicians or qualified healthcare professionals in hospitals, clinics, ICUs, and emergency rooms. Provides real-time visualization of internal structures to assist in clinical diagnosis and evaluation. Supports needle guide bracket kits for interventional procedures. No contrast agents used.
## Clinical Evidence
No clinical data. Bench testing performed including electrical safety (IEC 60601-1), electromagnetic compatibility (IEC 60601-1-2), acoustic output (per 2008 FDA guidance), and biocompatibility (ISO 10993-1, 5, 10).
## Technological Characteristics
Portable ultrasound system with main unit and array transducers (linear, convex, microconvex). Frequency range 2.0-10.0 MHz. Display modes: B, 2B, 4B, M, B+M. Software-controlled. Complies with IEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, and ISO 10993 standards.
## Regulatory Identification
An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
## Special Controls
*Classification.* Class II (special controls). A biopsy needle guide kit intended for use with an ultrasonic pulsed echo imaging system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.
## Predicate Devices
- Digital Ultrasonic Diagnostic Imaging System ([K091680](/device/K091680.md))
## Submission Summary (Full Text)
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Digital Ultrasonic Diagnostic Imaging System
510K Submission
OCT 12 2012
# Section 5- 510(k) Summary of Safety and Effectiveness
Prepared in accordance with the requirements of 21 CFR Part 807.92
1. Submitter:
Edan Instruments, Inc.
3/F-B, Nanshan Medical Equipments Park, Nanhai Rd 1019#, Shekou, Nanshan Shenzhen, 518067 P.R. China
Telephone: 0086-755-6856469
Fax: 0086-755-26882223
Contact Person: Randy Jiang Prepare date: Feb 21, 2012
2. Device name and Device name: Digital Ultrasonic Diagnostic Imaging System classification:
### Models D3 and D6
Classification: 892.1560 System, Imaging, Pulsed echo, Ultrasonic
#### Product code: IYO
892.1570 Transducer, Ultrasonic, Diagnostic
#### Product code: ITX
Regulatory Class: Class II
3. Predicate Device:
Digital Ultrasonic Diagnostic Imaging System. K091680 Manufacturer: Edan Instruments, Inc.
4. Device Description: D3 and D6 Digital Ultrasound Diagnostic Imaging System is a portable digital ultrasonic diagnostic system applied in ultrasound diagnostic examination of abdominal, obstetrical, small parts, gynecological, orthopedic, cardiac, and urological applications.
It is designed to produce ultrasound waves into body tissue and to present the returned echo information on the monitor, the resulting information is displayed in five display modes: B-Mode, 2B-Mode, 4B-Mode, M-Mode, B+M Mode. This system controlled by software is a Track 1 device that employs an array of probes that include linear array, convex linear array, microconvex linear array, transrectal and transvaginal with a frequency range of approximately 2.0MHz-10.0MHz.
The system consists of a main unit, transducers and other accessories.
{1}------------------------------------------------
#### 5. Intended Use:
The D3 and D6 Digital Ultrasonic Diagnostic Imaging System are applicable for adult or children ultrasound evaluation in hospitals, clinics, gynecology rooms, obstetrics rooms, examination rooms, intensive care units, and emergency rooms The D3 and D6 are intended for use by or on the order of a physician or similarly qualified health care professional for ultrasound evaluation of Fetus; Abdomen; Pediatrics; Small Organ; Neonatal head; Cardiology; Peripheral Vessel; Musculo-skeleton (both Conventional and Superficial); Urology (including prostate); Transrecta and Transvagina.
#### 6. Effectiveness and Safety Considerations:
#### Clinical test:
Clinical testing is not required.
#### Non-clinical test:
The following safety standards are conducted on the subject device:
- 1. IEC 60601-1 Electrical Safety
- 2. IEC 60601-1-2 Electromagnetic Compatibility
- 3. Acoustic output testing as per the guideline "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers" dated September 9, 2008.
- 4. UD-2, IEC 60601-2-37
- 5. ISO 10993-1, ISO 10993-5 and ISO 10993-10
### 7.Comparison to the predicate device
Comparison to the predicate device, the subject device has the similar technology characteristics and has the same intended use, same design principle, same electrical classification and same accuracy. The different between the subject device and predicate device primarily includes physical specifications, display type and display mode, all the above differences do not affect the usage, safety and effectiveness, and no new question is raised regarding the safety and effectiveness.
## 8. Substantially Equivalent Determination
Verification and validation testing was conducted on the subject device. This premarket notification submission demonstrates that D3 and D6 Digital Ultrasonic Diagnostic Imaging System is substantially equivalent to the predicate device.
{2}------------------------------------------------
#### DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three tail feathers, representing the department's commitment to health, human services, and well-being. The eagle is surrounded by a circular inscription that reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA".
#### Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993
OCT 12 2012
Edan Instruments, Inc. % Mr. Ned Devine Senior Staff Engineer/FDA Office Coordinator Underwriters Laboratories, Inc. 333 Pfingsten Road NORTHBROOK IL 60062
. Re: K122574
Trade/Device Name: Digital Ultrasonic Diagnostic Imaging System, Models D3 and D6 Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulatory Class: II Product Code: IYO and ITX Dated: September 21, 2012 Received: September 26, 2012
Dear Mr. Devine:
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 Digital Ultrasonic Diagnostic Imaging System, Models D3 and D6, as described in your premarket notification:
Transducer Model Number
| D3 | D6 |
|-------------|--------|
| C361-1/C341 | C363-1 |
| C321-1 | C362 |
| L741 | C343-1 |
| E741 | C321 |
| E611-1 | L743 |
| | E743 |
| | E613 |
{3}------------------------------------------------
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 (OS) 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 Shahram Vaezy at (301) 796-6242.
Sincerely Yours,
Zumhof D O'Hern Lier
Janine M. Morris Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health
Enclosure(s)
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## Section 6- Indications for Use
510(k) Number (if known):
Device Name: Digital Ultrasonic Diagnostic Imaging System Models D3 and D6
The D3 and D6 Digital Ultrasonic Diagnostic Imaging System are applicable for adult or children ultrasound evaluation in hospitals, clinics, gynecology rooms, obstetrics rooms, examination rooms, intensive care units, and emergency rooms The D3 and D6 are intended for use by or on the order of a physician or similarly qualified health care professional for ultrasound evaluation of Fetus; Abdomen; Pediatrics; Small Organ; Neonatal head; Cardiology; Peripheral Vessel; Musculo-skeleton (both Conventional and Superficial); Urology (including prostate); Transrecta and Transvagina.
Prescription Use (21 CFR Part 801 Subpart D)
Or Over the Counter Use
(21 CFR Part 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IFNEEDED)
Concurrence of CDRH, Office of In Vitro Diagnostic Device Evaluation and Safety (OIVD)
(Division Sign-Off)
Division of Radiotogical Devices Office of In Vitro Diagnostic Device Evaluation and Safety
Ki22574
510K.
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## Diagnostic Ultrasound Indications for Use Form
## D3 Digital Ultrasonic Diagnostic Imaging System
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 Doppler | Combined (Specify) | Other* (Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | N | N | | | | N | Note 1,Noter2 |
| Abdominal | N | N | | | | N | Note 1,Noter2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | N | N | | | | N | Note 1,Noter2 |
| Small Organ (Specify) | N | N | | | | N | Note 1,Noter2 |
| Neonatal Cephalic | N | N | | | | N | Note 1,Noter2 |
| Adult Cephalic | | | | | | | |
| Transrectal | N | N | | | | N | Note 1,Noter2 |
| Transvaginal | N | N | | | | N | Note 1,Noter2 |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | N | N | | | | N | Note 1,Noter2 |
| Musculo-skeletal (Superficial) | N | N | | | | N | Note 1,Noter2 |
| Intravascular | | | | | | | |
| Other (Gynecology) | N | N | | | | N | |
| Cardiac | N | N | | | | N | Note 1,Noter2 |
| Intravascular | | | | | | | |
| Peripheral vascular | N | N | | | | N | Note 1,Noter2 |
| Other (Urology) | N | N | | | | N | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Mull D'the
(Division Sign-Off)
Division of Radiological Devices
Office In Vitro Diagnostic Device Evaluation and Safety
510K K122574/
{6}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
### D3 with C361-1 / C341 Transducer
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| | Mode of Operation | | | | | | |
|---------------------------------|-------------------|---|-----|-----|---------------|--------------------|---------------------|
| Clinical Application | B | M | PWD | CWD | Color Doppler | Combined (Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | P | P | | | | P | Note 1,Noter2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | P | P | | | | P | |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
(Division Sign-Off)
Division of Radiological Devices Office of In Vitro Diagnostic Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K K122574
{7}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
## D3 with C321-1 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
Doppler | Combined
(Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | P | P | | | | P | Note 1,Noter2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | P | P | | | | P | Note 1,Noter2 |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | P | P | | | | P | Note 1,Noter2 |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
510K -
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Office of In Vitro Diagnostic Device Evaluation and Safety
Division of Radiological Devices
(Division Sign-Off)
6-4
{8}------------------------------------------------
## Diagnostic Ultrasound Indications for Use Form
## D3 with L741 Transducer
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | Mode of Operation | | | | | | Other*
(Specify) |
|---------------------------------|--|-------------------|---|-----|-----|------------------|-----------------------|---------------------|
| | | B | M | PWD | CWD | Color
Doppler | Combined
(Specify) | |
| Ophthalmic | | | | | | | | |
| Fetal / Obstetrics | | | | | | | | |
| Abdominal | | | | | | | | |
| Intra-operative (Specify) | | | | | | | | |
| Intra-operative (Neurological) | | | | | | | | |
| Laparoscopic | | | | | | | | |
| Pediatric | | | | | | | | |
| Small Organ (Specify) | | P | P | | | | P | Note 1,Noter2 |
| Neonatal Cephalic | | P | P | | | | P | Note 1,Noter2 |
| Adult Cephalic | | | | | | | | |
| Transrectal | | | | | | | | |
| Transvaginal | | | | | | | | |
| Transurethral | | | | | | | | |
| Musculo-skeletal (Conventional) | | P | P | | | | P | Note 1,Noter2 |
| Musculo-skeletal (Superficial) | | P | P | | | | P | Note 1,Noter2 |
| Intravascular | | | | | | | | |
| Other (Gynecology) | | | | | | | | |
| Cardiac | | | | | | | | |
| Intravascular | | | | | | | | |
| Peripheral vascular | | P | P | | | | P | Note 1,Noter2 |
| Other (Urology) | | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
Small organ includes galactophore, thyroid gland, prostate
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
(Division Sign-Off)
Division of Radiological Devices Office of In Vitro Diagnostic Devices
Office of In Vitro Diagnostic Devices
Office of In Vitro Diagnostic Devices
510k K122574
{9}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
## D3 with E741 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
Doppler | Combined
(Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | | | | | | | |
| Abdominal | | | | | | | |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | | | | | | | |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | P | P | | | | P | Note 1,Noter2 |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | | | | | | | |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
*(Division Sign-Off)*
Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety
510K K12257X/
ર-ઉ
{10}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
## D3 with E611-1 Transducer
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | B | M | PWD | CWD | Color Doppler | Combined (Specify) | Other* (Specify) |
|---------------------------------|---|---|-----|-----|---------------|--------------------|------------------|
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | | | | | | | |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | | | | | | | |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | P | P | | | | P | Note 1,Noter2 |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
***(Division Sign Off)***
(Division Sign-Off) Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety
510K K122574/
{11}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
## D6 Digital Ultrasonic Diagnostic Imaging System
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
Doppler | Combined
(Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | N | N | | | | N | Note 1,Note2 |
| Abdominal | N | N | | | | N | Note 1,Note2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | N | N | | | | N | Note 1,Note2 |
| Small Organ (Specify) | N | N | | | | N | Note 1,Note2 |
| Neonatal Cephalic | N | N | | | | N | Note 1,Note2 |
| Adult Cephalic | | | | | | | |
| Transrectal | N | N | | | | N | Note 1,Note2 |
| Transvaginal | N | N | | | | N | Note 1,Note2 |
| Transurethral | | | | | | | |
| Musculo-skeletal
(Conventional) | N | N | | | | N | Note 1,Note2 |
| Musculo-skeletal (Superficial) | N | N | | | | N | Note 1,Note2 |
| Intravascular | | | | | | | |
| Other (Gynecology) | | | | | | | |
| Cardiac | N | N | | | | N | Note 1,Note2 |
| Intravascular | | | | | | | |
| Peripheral vascular | N | N | | | | N | Note 1,Note2 |
| Other (Urology) | N | N | | | | N | Note 1,Note2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(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 Radiological Devices Office of In Vitro Diagnostic Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K K122574/
{12}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
### D6 with C363-1 Transducer
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | | | | | | Other* (Specify) |
|---------------------------------|-------------------|---|-----|-----|---------------|---------------------|------------------|
| | B | M | PWD | CWD | Color Doppler | Combined (Specify). | |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | P | P | | | | P | Note 1,Noter2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | P | P | | | | P | Note 1,Noter2 |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
510K.
Prescription Use (Per 21 CFR 801.109)
Mmhnd DK
(Division Sign-Off)
Division of Radiological Devices
Vitro Diagnostic Devices Devices
Vitro Diagnostic Devices Custom Custom Office of In Vitro Diagnostic Devices
Office of In Vitro Diagnostic Devices
Constitution Diagnostic Devices Evelulation and Safety
Constitution of One Commend Safety
6-9
{13}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
## D6 with C362 Transducer
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | | | | | | Other*
(Specify) |
|---------------------------------|-------------------|---|-----|-----|---------------|-----------------------|---------------------|
| | B | M | PWD | CWD | Color Doppler | Combined
(Specify) | |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Note2 |
| Abdominal | P | P | | | | P | Note 1,Note2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | P | P | | | | P | Note 1,Note2 |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Note2 |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Note2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(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 Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K K122574
{14}------------------------------------------------
## Diagnostic Ultrasound Indications for Use Form
### D6 withC343-1 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
Doppler | Combined
(Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | P | P | | | | P | Note 1,Noter2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | P | P | | | | P | Note 1,Noter2 |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(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 Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K. K.122574/
{15}------------------------------------------------
## Diagnostic Ultrasound Indications for Use Form
## D6 with C321 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 Doppler | Combined (Specify) | Other* (Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | P | P | | | | P | Note 1,Noter2 |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | P | P | | | | P | Note 1,Noter2 |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | P | P | | | | P | Note 1,Noter2 |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
510K
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
*(Division Sign-Off)*
Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety
{16}------------------------------------------------
## Diagnostic Ultrasound Indications for Use Form
## D6 with L743 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
Doppler | Combined
(Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | | | | | | | |
| Abdominal | | | | | | | |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | | | | | | | |
| Small Organ (Specify) | P | P | | | | P | Note 1,Noter2 |
| Neonatal Cephalic | P | P | | | | P | Note 1,Noter2 |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | P | P | | | | P | Note 1,Noter2 |
| Musculo-skeletal (Superficial) | P | P | | | | P | Note 1,Noter2 |
| Intravascular | | | | | | | |
| Other (Gynecology) | | | | | | | |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | P | P | | | | P | Note 1,Noter2 |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
Small Organ includes galactophore, thyroid gland, prostate
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
510K.
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
MundlADR
(Division Sign-Off)
Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety
K122574
{17}------------------------------------------------
# Diagnostic Ultrasound Indications for Use Form
## D6 with E743 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
Doppler | Combined
(Specify) | Other*
(Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | | | | | | | |
| Abdominal | | | | | | | |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | | | | | | | |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | P | P | | | | P | Note 1,Noter2 |
| Transvaginal | | | | | | | |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | | | | | | | |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent.
Note 2: Needle guide bracket kit
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
---
(Division Sign-Off)
Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety
510K K12252/
{18}------------------------------------------------
## Diagnostic Ultrasound Indications for Use Form
### D6 with E613 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 Doppler | Combined (Specify) | Other* (Specify) |
| Ophthalmic | | | | | | | |
| Fetal / Obstetrics | P | P | | | | P | Note 1,Noter2 |
| Abdominal | | | | | | | |
| Intra-operative (Specify) | | | | | | | |
| Intra-operative (Neurological) | | | | | | | |
| Laparoscopic | | | | | | | |
| Pediatric | | | | | | | |
| Small Organ (Specify) | | | | | | | |
| Neonatal Cephalic | | | | | | | |
| Adult Cephalic | | | | | | | |
| Transrectal | | | | | | | |
| Transvaginal | P | P | | | | P | Note 1,Noter2 |
| Transurethral | | | | | | | |
| Musculo-skeletal (Conventional) | | | | | | | |
| Musculo-skeletal (Superficial) | | | | | | | |
| Intravascular | | | | | | | |
| Other (Gynecology) | P | P | | | | P | Note 1,Noter2 |
| Cardiac | | | | | | | |
| Intravascular | | | | | | | |
| Peripheral vascular | | | | | | | |
| Other (Urology) | P | P | | | | P | Note 1,Noter2 |
N = new indication; P = previously cleared by FDA; E = added under this appendix
Additional comments: Combined mode: B+M
Note 1: This feature does not use contrast agent ..
Note 2: Needle guide bracket kit.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use (Per 21 CFR 801.109)
Michael D. O'Brien
(Division Sign-Off)
Division of Radiological Devices Office of In Vitre Diagnostic Devices
Office of In Vitce Diagnostic Device Evaluation and Safety
510K K122574
---
**Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO/K122574](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO/K122574)
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