K Number
K121063
Device Name
VIVID S5 DIAGNOSTIC ULTRASOUND SYSTEM, VIVID S6 DIAGNOSTIC ULTRASOUND SYSTEM
Date Cleared
2012-08-21

(137 days)

Product Code
Regulation Number
892.1550
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/Obstetrics; Abdominal/Gynecology; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transesophageal; Transrectal; Transvaginal; and Intraoperative (abdominal, thoracic, and vascular).
Device Description
The Vivid S5 and Vivid S6 are mobile ultrasound consoles having a wide assortment of electronic array transducers intended primarily for echocardiography with additional capability in vascular and general ultrasound imaging. Its intuitive user interface, high level of auto-optimization along with significantly reduced size and weight make it readily maneuverable, efficient and easy to use.
More Information

No
The document explicitly states "Mentions AI, DNN, or ML: Not Found" and the device description focuses on auto-optimization and user interface, not AI/ML capabilities.

No
Explanation: The device description and intended use clearly state that it is for "ultrasound evaluation" and "imaging," indicating a diagnostic rather than therapeutic purpose.

Yes

The 'Intended Use / Indications for Use' section states the device is for "ultrasound evaluation" and the 'Predicate Device(s)' section explicitly names "Vivid S5 and Vivid S6 Diagnostic Ultrasound Systems", indicating its diagnostic purpose.

No

The device description explicitly states it is a "mobile ultrasound console" with "electronic array transducers," indicating it is a hardware device that performs ultrasound imaging.

Based on the provided information, this device is not an IVD (In Vitro Diagnostic).

Here's why:

  • IVD Definition: In vitro diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections.
  • Device Function: The description clearly states that this device is a mobile ultrasound console used for ultrasound evaluation of various anatomical sites. Ultrasound is an imaging modality that uses sound waves to create images of internal body structures. It does not involve testing samples taken from the body.
  • Intended Use: The intended use describes diagnostic imaging procedures performed directly on the patient.

Therefore, this device falls under the category of medical imaging devices, not in vitro diagnostics.

N/A

Intended Use / Indications for Use

The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/Obstetrics; Abdominal/Gynecology; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transesophageal; Transrectal; Transvaginal; and
The Vivid S5/S6 ultrasound systems are intended for use by, or under the direction of, a qualified physicain for untrasound maging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transesophageal; Transrectal; Transvaginal; and Intraoperative (abdominal, thoracic, and vascular).

Product codes (comma separated list FDA assigned to the subject device)

IYN, IYO, ITX, LLZ

Device Description

The Vivid S5 and Vivid S6 are mobile ultrasound consoles having a wide assortment of electronic array transducers intended primarily for echocardiography with additional capability in vascular and general ultrasound imaging. Its intuitive user interface, high level of auto-optimization along with significantly reduced size and weight make it readily maneuverable, efficient and easy to use.

Mentions image processing

Not Found

Mentions AI, DNN, or ML

Not Found

Input Imaging Modality

Ultrasound

Anatomical Site

Fetal/Obstetrics, Abdominal/Gynecology, Pediatric, Small Organ (breast, testes, thyroid), Neonatal Cephalic, Adult Cephalic, Cardiac (adult and pediatric), Peripheral Vascular, Musculo-skeletal Conventional, Musculo-skeletal Superficial, Urology (including prostate), Transesophageal, Transrectal, Transvaginal, Intraoperative (abdominal, thoracic, and vascular).

Indicated Patient Age Range

Adult and Pediatric

Intended User / Care Setting

Qualified physician

Description of the training set, sample size, data source, and annotation protocol

Not Found

Description of the test set, sample size, data source, and annotation protocol

Not Found

Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)

The subject of this premarket submission, the modified Vivid S5/S6, did not require clinical studies to support substantial equivalence.

Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)

Not Found

Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.

K102393, K101149

Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.

K101149, K071985, K092079, K082374, K113690

Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).

Not Found

§ 892.1550 Ultrasonic pulsed doppler imaging system.

(a)
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.(b)
Classification. Class II.

0

K121063

GE Healthcare

510(k) Premarket Notification Submission
Vivid S5/S6 Ultrasound System

510(k) Summary

In accordance with 21 CFR 807.92 the following summary of information is provided:
Date:5 April 2012AUG 2 1 2012
Submitter:GE Healthcare
9900 Innovation Dr
Wauwatosa, WI 53226
Primary Contact Person:Bryan Behn
Regulatory Affairs Manager
GE Healthcare, [GE Medical Systems Ultrasound and Primary Care
Diagnostics, LLC]
T:(414)721-4214
F:(414)918-8275
Secondary Contact Person:Carmel Lehrer
Regulatory Affairs Specialist
GE Medical Systems Israel Ltd.
T:+972-4-8419-534
F:+972-4-8419-500
Device: Trade Name:Vivid S5 and Vivid S6 Diagnostic Ultrasound System
Common/Usual Name:Vivid S5, Vivid S6
Classification Names:Class II
Product Code:Ultrasonic Pulsed Doppler Imaging System, 21 CFR 892.1550, 90-IYN
Ultrasonic Pulsed Echo Imaging System, 21 CFR 892.1560, 90-IYO
Predicate Device(s):Vivid S5 and Vivid S6 Diagnostic Ultrasound Systems, K102393.
Vivid E9 Diagnostic Ultrasound System, K101149.
Device Description:The Vivid S5 and Vivid S6 are mobile ultrasound consoles having a
wide assortment of electronic array transducers intended primarily for
echocardiography with additional capability in vascular and general
ultrasound imaging. Its intuitive user interface, high level of auto-
optimization along with significantly reduced size and weight make
it readily maneuverable, efficient and easy to use.
Intended Use:The device is intended for use by a qualified physician for ultrasound
evaluation of Fetal/Obstetrics; Abdominal/Gynecology; Pediatric;
Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult
Cephalic; Cardiac (adult and pediatric); Peripheral Vascular;
Musculo-skeletal Conventional and Superficial; Urology (including
prostate); Transesophageal; Transrectal; Transvaginal; and

1

Image /page/1/Picture/1 description: The image shows a circular logo with the letters 'GE' intertwined in the center. The letters are stylized with curved lines and loops, creating a flowing and interconnected design. The logo is enclosed within a circle that has a textured or patterned border, adding a decorative element to the overall design. The image is in black and white.

Technology: The modified Vivid S5/S6 employs the same fundamental scientific technology as its predicate devices.

Determination of Substantial Equivalence:

Summary of Non-Clinical Tests:

The device has been evaluated for acoustic output, biocompatibility, cleaning and disinfection effectiveness as well as thermal, electrical, electromagnetic, and mechanical safety, and has been found to conform with applicable medical device safety standards. The modified Vivid S5/S6 and its applications comply with voluntary standards as detailed in Section 9, 11 and 17 of this premarket submission. The following quality assurance measures were applied to the development of the system:

  • Risk Analysis ●
  • Requirements Reviews .
  • Design Reviews .
  • Testing on unit level (Module verification) .
  • . Integration testing (System verification)
  • Final Acceptance Testing (Validation) .
  • . Performance testing (Verification)
  • Safety testing (Verification) .

Transducer materials and other patient contact materials are biocompatible.

Summary of Clinical Tests:

The subject of this premarket submission, the modified Vivid S5/S6, did not require clinical studies to support substantial equivalence.

GE Healthcare considers the modified Vivid S5/S6 to be as safe, and effective as the predicate device(s). The performance of the modified Vivid S5/S6 is substantially equivalent to the predicate device(s).

Intended uses and other key features are consistent with traditional clinical practice, FDA guidelines, and established methods of patient examination. The design and development process of the manufacturer conforms with 21 CFR 820, and ISO13485 quality systems. The device conforms to applicable medical device safety standards and compliance is verified through independent evaluation with ongoing factory surveillance. Diagnostic ultrasound has accumulated a long history of safe and effective performance. Therefore, it is the opinion of GE Healthcare that the Vivid S5/S6 Diagnostic Ultrasound is substantially equivalent with respect to safety and effectiveness to devices currently cleared for market.

Conclusion:

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 or bird-like figure with three curved lines representing its wings or body. The bird is positioned to the right of a circular arrangement of text that reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA". The text is arranged around the circumference of the circle.

Food and Drug Administration

10903 New Hampshire Avenue Silver Spring, MD 20993

AUG 2 1 2012

GE Medical Systems Israel Ltd. % Mr. Bryan Behn Regulatory Affairs Manager GE Healthcare 9900 Innovation Drive WAUWATOSA WI 53226

Re: K121063

Trade/Device Name: Vivid S5/S6 Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: IYN, IYO, ITX, and LLZ Dated: August 10, 2012 Received: August 13, 2012

Dear Mr. Behn:

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 Vivid S5/S6, as described in your premarket notification:

Transducer Model Number

38-RS108-RSE8C-RS6Tc/6Tc-RS
3Sc-RS12S-RS8L-RS6T/6T-RS
58-RSM4S-RS9L-RS9T/9T-RS
68-RS .4C-RS12L-RSP2D
78-RS8C-RSi12L-RSP6D

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 (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 Jeffrey Ballyns at (301) 796-6105.

Sincerely Yours,

Marlon Dóthan for

Janine M. Morris Acting 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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510(k) Number (if known):

Device Name: Vivid S5/S6

Indications for Use:

The current modifications do not change the indications for use. As previously reported and cleared, the Vivid S5/S6 ultrasound systems are intended for use by, or under the direction of, a qualified the Vira 65/00 and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small physiolan for untrasound maging and Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Organ (vertes), Musculo-skeletal Conventional and Superficial; Urology (including prostate); I cripiteral Vascular, Museulo Skelear Senal; and Intraoperative (abdominal, thoracic, and vascular).

Prescription Use_ X (Part 21 CFR 801 Subpart D) AND/OR

Over-The-Counter Use (Part 21 CFR 801 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)

A. Shard D. O'Hern

(Division Sign-Off) Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety

510(k) Number K121063

5

Image /page/5/Picture/0 description: The image shows a black and white logo of General Electric (GE). The logo consists of the letters 'G' and 'E' intertwined in a stylized, cursive font. The letters are enclosed within a circular border that has a decorative, swirling pattern around the edges.

Indications for Use Forms

The following forms represent indications with clinical applications and exam types along with the modes of operation for the Vivid S5/S6 system and for all of its probe/mode combinations. Combinations identified by "P" represent those previously FDA cleared. In a similar manner "N" represents a new mode or application being added as new to the system or a transducer in this submission. In a similar manner, "E" represents combinations added to the unmodified device via Guidance Appendix E. This modification did not alter the previously cleared system level indications, clinical applications or modes of operation.

Indications for Use tables' headings, legends and footers taken from all previous submissions, are aligned to the same unified format.

Pencil probes

PW mode of operation, which was previously included in error for the Pencil probes; P2D and P6D, has been removed from their Indications for Use forms.

128-RS

The 12S-RS is identical to the 12S-D previously cleared on the Vivid E9 K101149 with a change to the -RS laptop/small console connector instead of the -D large console connector. Clinical applications and modes of operation are as in 12S-D. Additional Abdominal Vascular applications are added to 12S-RS based on clearance of these applications on other transducers (10S-RS and 7S-RS) previously cleared on Vivid S5/S6 (K071985, K092079) and Vivid i/q (K082374).

Transducers added via Appendix E: 3Sc-RS

One transducer has been added via Appendix E of the Ultrasound Guidance since the previous clearance. Transducer 3Sc-RS, which is similar to the previously cleared 3S-RS with a few minor improvements.

6

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 Diagnostic Ultrasound System

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/ObstetricsPPPPPPPPPPP
Abdominal[1]PPPPPPPPPPP
PediatricPPPPPPPPPPP
Small Organ (specify)[2]PPPPPPPPPPP
Neonatal CephalicPPPPPPPPPPP
Adult CephalicPPPPPPPPPPP
Cardiac [3]PPPPPPPPPPP
Peripheral VascularPPPPPPPPPPP
Musculo-skeletal ConventionalPPPPPPPPPP
Musculo-skeletal SuperficialPPPPPPPPPP
Other[4]PPPPPPPPPPP
Exam Type, Means of Access
TransesophagealPPPPPPPPPP
TransrectalPPPPPPPPPP
TransvaginalPPPPPPPPPP
Transuretheral
Intraoperative (specify)[5]PPPPPPPPPP
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

  • [1] Abdominal includes GYN/Pelvic and Renal.
  • [2] Small organ includes breast, testes, thyroid.
  • [3] Cardiac is Adult and Pediatric.
  • [4] Other use includes Urology.
  • [5] Intraoperative includes abdominal, thoracic (cardiac), and vascular (PV).
  • [*] Combined modes are BIM, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD,

રીભ

  • [�] Coded Pulse is for digitally encoded harmonics.
    (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

(Division Slan of Radiological

Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)

Prescription Use (Per 21 CFR 801.109)

7

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Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 3S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/ObstetricsPPPPPPPPPPP
Abdominal[1]PPPPPPPPPPP
PediatricPPPPPPPPPPP
Small Organ (specify)
Neonatal Cephalic
Adult CephalicPPPPPPPPPPP
Cardiac[2]PPPPPPPPPPP
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other[3]PPPPPPPPPPP
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

[3] Other use includes Urology.

[0] Other use Includes Grology:
[*] Combined modes are BIM, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD,

[♦] Coded Pulse is for digitally encoded harmonics.

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
(Division Sign-Off)
Prescription Use (Per 21 CFR 801.109)Division of Radiological Devices
510kK191063

8

Image /page/8/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The logo is in black and white.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 3Sc-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse®Other
Ophthalmic
Fetal/ObstetricsmEEEEEEEE
Abdominal[1]EEEEEEEEE.U
PediatricEEEEEEEEE
Small Organ (specify)
Neonatal Cephalic
Adult CephalicEEEEEEEE
Cardiac(2)EEEEEEEEEE
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
OlbergiEEEEEEEട്E
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

[3] Other use includes Urology.

[0] Other use included Grology.
[*] Combined modes are B/M, B/PWD, B/CWD, B/Color/PWD, B/Color/PWD, B/Power/PWD.

[+] Coded Pulse is for digitally encoded harmonics.

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
(Division Sign-Off)
Prescription Use (Per 21 CFR 801,109) Division of Radiological Devices
510kK121063

9

Image /page/9/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined in a stylized, cursive font. The letters are enclosed within a circular border. The logo is black and white.

510(k) Premarket Notification Submission April 5, 2012 Vivid S5/S6 Ultrasound System

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 5S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

| Clinical Application
Anatomy/Region of Interest | B | M | PW
Doppler | CW
Doppler | Color
Doppler | Color M
Doppler | Power
Doppler | Combined
Modes* | Harmonic
Imaging | Coded
Pulse* | Other |
|----------------------------------------------------|---|---|---------------|---------------|------------------|--------------------|------------------|--------------------|---------------------|-----------------|-------|
| Ophthalmic | | | | | | | | | | | |
| Fetal/Obstetrics | P | P | P | P | P | P | P | P | P | P | |
| Abdominal[1] | P | P | P | P | P | P | P | P | P | P | |
| Pediatric | P | P | P | P | P | P | P | P | P | P | |
| Small Organ (specify) | | | | | | | | | | | |
| Neonatal Cephalic | | | | | | | | | | | |
| Adult Cephalic | P | P | P | P | P | P | P | P | P | P | |
| Cardiac[2] | P | P | P | P | P | P | P | P | P | P | |
| Peripheral Vascular | | | | | | | | | | | |
| Musculo-skeletal Conventional | | | | | | | | | | | |
| Musculo-skeletal Superficial | | | | | | | | | | | |
| Other | | | | | | | | | | | |
| Exam Type, Means of Access | | | | | | | | | | | |
| Transesophageal | | | | | | | | | | | |
| Transrectal | | | | | | | | | | | |
| Transvaginal | | | | | | | | | | | |
| Transuretheral | | | | | | | | | | | |
| Intraoperative (specify) | | | | | | | | | | | |
| Intraoperative Neurological | | | | | | | | | | | |
| Intravascular | | | | | | | | | | | |
| Laparoscopic | | | | | | | | | | | |

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

[2] Cordiao is Addit and 7 Collutio:
[*] Combined modes are BIM, B/Color M, B/PWD, B/CWD, B/Color/PWD, B/Power/PWD.

[♦] Coded Pulse is for digitally encoded harmonics.

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH/ Office of In Vitro Diagnostic Devices (OIVD)
(Division Sign-Off)
Prescription Use (Per 21 CFR 801.109)
Division of Radiological Devices
510kK121063
OIVD

10

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510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 6S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/ObstetricsPPPPPPPPPP
Abdominal[1]PPPPPPPPPP
PediatricPPPPPPPPPP
Small Organ (specify)
Neonatal CephalicPPPPPPPPPP
Adult Cephalic
Cardiac[2]PPPPPPPPPP
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

[2] Combined modes are BIM, B/PWD, B/CWD, B/Color/PWD, B/Color/PWD, B/Power/PWD.

[♦] Coded Pulse is for digitally encoded harmonics.

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
Prescription Use (Per 21 CFR 801.109)
(Division Sign-Off)
Division of Radiological Devices
510kDIVD

11

Image /page/11/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters "GE" intertwined within a circular border. The design is simple and recognizable, representing the company's brand identity.

510(k) Premarket Notification Submission April 5, 2012 Vivid S5/S6 Ultrasound System

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 7S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal[1]PPPPPPPPPP
PediatricPPPPPPPPPP
Small Organ (specify)
Neonatal CephalicPPPPPPPPPP
Adult Cephalic
Cardiac[2]PPPPPPPPPP
Peripheral VascularPPPPPPPPPP
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other[3]PPPPPPPPPP
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

[3] Other use includes Urology.

[0] Other boo included Crelogy.
[*] Combined modes are BIM, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD.

[�] Coded Pulse is for digitally encoded harmonics.

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Prescription Use (Per 21 CFR 801.109)
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510k

12

Image /page/12/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters "G" and "E" intertwined within a circular border. The letters are stylized and appear to be in a cursive or script font. The logo is black and white.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 10S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal[1]PPPPPPPPPP
PediatricPPPPPPPPPP
Small Organ (specify)
Neonatal CephalicPPPPPPPPPP
Adult CephalicPPPPPPPPPP
Cardiac[2]PPPPPPPPPP
Peripheral VascularPPPPPPPPPP
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

  • [1] Abdominal includes GYN/Pelvic and Renal.
    [2] Cardiac is Adult and Pediatric.

  • [2] Combined modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD,

  • Leoded Bolse is for digitally encoded harmonics.

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210k

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Prescription Use (Per 21 CFR 801.109)

13

Image /page/13/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The letters are stylized with curved lines, and the border has a textured appearance.

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 12S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
PulseOther
Ophthalmic
Fetal/Obstetrics
Abdominal[1]NNNNNNNNN
PediatricNNNNNNNNN
Small Organ (specify)
Neonatal CephalicNNNNNNNNN
Adult Cephalic
Cardiac[2]NNNNNNNNN
Peripheral VascularNNNNNNNNN
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

[2] Combined modes are BIM, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD,

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Division of Radiological Devices

510k

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Prescription Use (Per 21 CFR 801.109)

14

Image /page/14/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The letters are stylized and appear to be hand-drawn or calligraphic. The logo is black and white.

510(k) Premarket Notification Submission April 5, 2012 Vivid S5/S6 Ultrasound System

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with M4S-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/ObstetricsPPPPPPPPPP
Abdominal[1]PPPPPPPPPP
PediatricPPPPPPPPP
Small Organ (specify)
Neonatal Cephalic
Adult CephalicPPPPPPPPPP
Cardiac[2]PPPPPPPPPP
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Cardiac is Adult and Pediatric.

(2) Carthat is Adult and Pediatio
[*] Combined modes are B/M, B/Color M, B/PWD, B/CWD, B/Color/PWD, B/Power/PWD.

(+] Coded Pulse for digitally encoded harmonics.

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Division of Radiological Devices

510K

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15

Image /page/15/Picture/1 description: The image shows a logo with the letters 'GE' intertwined within a circle. The letters are stylized and appear to be hand-drawn or calligraphic. The logo is black and white, with the letters and the outline of the circle in black against a white background. The logo is a vintage design, likely representing the General Electric company.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 4C-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/ObstetricsPPPPPPPPP
Abdominal[1]PPPPPPPPP
PediatricPPPPPPPPP
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic
Cardiac
Peripheral VascularPPPPPPPPP
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other[2]PPPPPPPPP
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Other use includes Urology.

  1. Oner use Includes Orology.
    *] Combined modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD.

↑ | Geden Bulse is for digitally encoded harmonics.

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16

Image /page/16/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters "GE" intertwined within a circular border. The letters are stylized and connected, creating a distinctive monogram. The logo is in black and white.

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 8C-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal[1]PPPPPPPPP
PediatricPPPPPPPPP
Small Organ (specify)[2]PPPPPPPPP
Neonatal CephalicPPPPPPPPP
Adult Cephalic
Cardiac[3]PPPPPPPPP
Peripheral VascularPPPPPPPPP
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

  • [1] Abdominal includes GYN/Pelvic and Renal.
  • [2] Small organ includes breast, testes, thyroid.

[3] Cardiac is Adult and Pediatric.

[0] Combined modes are B/M, B/PWD, B/CWD, B/Color/PVWD, B/Power/PWD,

  • Coded Pulse is for digitally encoded harmonics.
    (Division Sign-Off)
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17

Image /page/17/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The logo is in black and white.

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with E8C-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/ObstetricsPPPPPPPPP
Abdominal[1]PPPPPPPPP
Pediatric
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic
Cardiac
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other[2]PPPPPPPPP
Exam Type, Means of Access
Transesophageal
TransrectalPPPPPPPPP
TransvaginalPPPPPPPPP
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Other use includes Urology.

[2] Other use induded Orology.
[1] Combined modes are BIM, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD.

Coded Pulse is for digitally encoded harmonics.

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Division of Radiological Devices
510k 6/2/03

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18

Image /page/18/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The letters are stylized and appear in a bold, sans-serif font, creating a recognizable and iconic emblem for the company.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 8L-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal[1]PPPPPPPPP
PediatricPPPPPPPPP
Small Organ (specify)[2]PPPPPPPPP
Neonatal Cephalic
Adult Cephalic
Cardiac
Peripheral VascularPPPPPPPPP
Musculo-skeletal ConventionalPPPPPPPPP
Musculo-skeletal SuperficialPPPPPPPPP
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Small organ includes breast, testes, thyroid.

[*] Combined modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Color/PWD, B/Power/PWD.

() Coded Puls is for digitally encoded harmonics.

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510k K121063 OIVD

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19

Image /page/19/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters "GE" intertwined within a circular border. The letters and the border are in black, contrasting with the white background.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 9L-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal[1]PPPPPPPPPP
PediatricPPPPPPPPPP
Small Organ (specify)[2]PPPPPPPPPP
Neonatal Cephalic
Adult Cephalic
Cardiac
Peripheral VascularPPPPPPPPPP
Musculo-skeletal ConventionalPPPPPPPPPP
Musculo-skeletal SuperficialPPPPPPPPPP
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Abdominal includes GYN/Pelvic and Renal.

[2] Small organ includes breast, testes, thyroid.

Prescription Use (Per 21 CFR 801.109)

[*] Combined modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD, B/Power/PWD.

A Coded Pulse is for digitally encoded harmonics.

·

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510k K21063

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4-17

20

Image /page/20/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The letters and the border are black, creating a strong contrast against the white background.

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with 12L-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
PulseOther
Ophthalmic
Fetal/Obstetrics
AbdominalP*P*P*P*NP*P*P*P*
PediatricPPPPPPPPP
Small Organ (specify)[1]PPPPPPPPP
Neonatal Cephalic
Adult Cephalic
Cardiac
Peripheral VascularPPPPPPPPP
Musculo-skeletal ConventionalPPPPPPPPP
Musculo-skeletal SuperficialPPPPPPPPP
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)[2]PPPPPPPPP
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E (*Previously Cleared K113690)

Notes:

[1] Small organ includes breast, testes, thyroid.

  • [2] Intraoperative includes abdominal, thoracic (cardiac), and vascular (PV),
    [*] Combined modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD,

  • [] Øoded Pulse stor digitally encoded harmonics.


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K121063
510k

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21

Image /page/21/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters "G" and "E" intertwined within a circular border. The logo is black and white and appears to be a vintage version of the GE logo.

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with i12L-RS Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DoppterCombined
Modes*Harmonic
lmagingCoded
Pulse®Other
Ophthalmic
Fetal/Obstetrics
Abdomina [1]PPPPPPPPP
PediatricPPPPPPPPP
Small Organ (specify)[2]PPPPPPPPP
Neonatal Cephalic
Adult Cephalic
Cardiac(3)PPPPPPPPP
Peripheral VascularPPPPPPPPP
Musculo-skeletal ConventionalPPPPPPPPP
Musculo-skeletal SuperficialPPPPPPPPP
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)[4]PPPPPPPPP
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

  • [1] Abdominal includes GYN/Pelvic and Renal.
  • {2} Small organ includes breast, testes, thyroid.

[3] Cardiac is Adult and Pediatric.

[4] Intraoperative includes abdominal, thoracic (cardiac), and vascular (PV).

["] Combiged modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD,

[#] Cased Pulse is for digitally encoded harmonics.

Division of Radiological Devices

JK

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22

Image /page/22/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The logo is black and white.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 6Tc/6Tc-RS Transducer**

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal
Pediatric
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic
Cardiac[1]PPPPPPPPPP
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
TransesophagealPPPPPPPPPP
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1 Cardiac is Adult and Pediatric.

[*] Combined modes are B/M, B/Color M, B/PWD, B/Color/PWD, B/Power/PWD.

Coded Pulse is for digitally encoded harmonics.

67c differs from 6Tc-RS only in the connector type

Vocalmers to
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Division of Radiological Devices
510k K121028°3
OIVD

t
Children Children Children Charles (Children Charles) Children (Children) Children (Children) Children (Children) Children (Children) Children (Children) Children (C

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23

Image /page/23/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The design is simple and recognizable, representing the company's brand identity.

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 6T/ 6T-RS Transducer**

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal
Pediatric
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic
Cardiac[1]PPPPPPPPPP
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
TransesophagealPPPPPPPPPP
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Cardiac is Adult and Pediatric.

[1] Combined modes are B/M, B/Color M, B/PWD, B/CWD, B/Color/PWD, B/Power/PWD.

· ] Coded Pulse is for digitally encoded harmonics.

of colfiers from 6Tc-RS only in the connector type

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510k K121063

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24

Image /page/24/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The logo is black and white, with the letters and border appearing in black against a white background.

510(k) Premarket Notification Submission Vivid S5/S6 Ultrasound System April 5, 2012

Diagnostic Ultrasound Indications for Use Form GE Vivid S5/S6 with 9T/ 9T-RS Transducer**

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
Modes*Harmonic
ImagingCoded
Pulse*Other
Ophthalmic
Fetal/Obstetrics
Abdominal
Pediatric
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic ·
Cardiac[1]PPPPPPPPPP
Peripheral Vascular
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
TransesophagealPPPPPPPPPP
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:

[1] Cardiac is Adult and Pediatric.

(*) Combined modes are B/M, B/Color M, B/PWD, B/CWD, B/Color/PWD, B/Power/PWD.

(�] Coded Pulse is for digitally encoded harmonics.

differs fromy9T-RS only in the connector type

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25

Image /page/25/Picture/1 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a circular border. The letters and the border are in black, contrasting with the white background.

510(k) Premarket Notification Submission April 5, 2012 Vivid S5/S6 Ultrasound System

Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with P2D Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
ModesHarmonic
ImagingCoded
PulseOther
Ophthalmic
Fetal/Obstetrics
Abdominal
Pediatric
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic
Cardiac[1]P
Peripheral VascularP
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

Notes:
[1] Cardiac is Adult and Pediatric.

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510k K121063

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26

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Diagnostic Ultrasound Indications for Use Form

GE Vivid S5/S6 with P6D Transducer

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Mode of Operation
Clinical Application
Anatomy/Region of InterestBMPW
DopplerCW
DopplerColor
DopplerColor M
DopplerPower
DopplerCombined
ModesHarmonic
ImagingCoded
PulseOther
Ophthalmic
Fetal/Obstetrics
Abdominal
Pediatric
Small Organ (specify)
Neonatal Cephalic
Adult Cephalic
Cardiac [1]P
Peripheral VascularP
Musculo-skeletal Conventional
Musculo-skeletal Superficial
Other
Exam Type, Means of Access
Transesophageal
Transrectal
Transvaginal
Transuretheral
Intraoperative (specify)
Intraoperative Neurological
Intravascular
Laparoscopic

N = new indication; P = previously cleared by FDA; E = added under Appendix E

. : :

Notes:
[1] Cardiac is Adult and Pediatric.

(Division Sign-Off)
Division of Radiological Devices
510k K121063
(PLEAS

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)