Vivid E80/ Vivid E90/ Vivid E95

K202658 · GE Medical Systems Ultrasound and Primary Care Diagnostics · IYN · Mar 5, 2021 · Radiology

Device Facts

• Record ID: K202658
• Device Name: Vivid E80/ Vivid E90/ Vivid E95
• Applicant: GE Medical Systems Ultrasound and Primary Care Diagnostics
• Product Code: IYN · Radiology
• Decision Date: Mar 5, 2021
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.1550
• Device Class: Class 2
• Attributes: Pediatric

Intended Use

Vivid E80 / Vivid E90 / Vivid E95 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified and trained physician for ultrasound imaging, measurement, display and analysis of the human body and fluid. The device is intended for use in a hospital environment including echo lab, other hospital settings, operating room, Cath lab and EP lab or in private medical offices. The systems support the following clinical applications: Fetal/Obstetrics, Abdominal (including renal, GYN), Pediatric, Small Organ (breast, testes, thyroid), Neonatal Cephalic, Cardiac (adult and pediatic), Peripheral Vascular, Musculo-sketal Conventional, Musculo-skeletal Superficial, Urology (including prostate), Transvaginal, Transvaginal, Transrectal, Interventional Guidance (including Biopsy, Vascular Access), Intra-cardiac, Intra-luminal and Intraoperative (vascular). Modes of operation include: 3D, Real time (RT) 3D Mode (4D), B, M, PW Doppler, CW Doppler, Color M Doppler, Power Doppler, Harmonic Imaging, Coded Pulse and Combined modes: B/M, B/Color M, B/PWD or CWD, B/Color/PWD or CWD, B/Power/PWD.

Device Story

Mobile diagnostic ultrasound system for cardiac, vascular, and general radiology imaging. Inputs: ultrasound data from electronic array transducers (linear, curved, sector/phased, matrix, dual, CW, real-time 3D). System processes signals via internal electronics and software to produce 2D/3D/4D images, Doppler measurements, and analysis. Used in hospitals (OR, Cath/EP labs, echo labs) and private offices by physicians/trained clinicians. Output displayed on integrated OLED/LCD monitor; supports image storage, printing, and network connectivity (LAN/wireless). Provides real-time visualization and quantitative data to assist clinicians in diagnosis and interventional guidance. Includes authentication tool for ICE catheters. Benefits include non-invasive diagnostic imaging and procedural guidance.

Clinical Evidence

No clinical data. Substantial equivalence supported by bench testing, including acoustic output, biocompatibility, cleaning/disinfection effectiveness, and thermal/electrical/electromagnetic/mechanical safety testing per AAMI/ANSI ES60601-1, IEC 60601-1-2, IEC 60601-2-37, ISO 10993-1, and IEC 62359.

Technological Characteristics

Mobile console with height-adjustable control panel, color LCD touch panel, and OLED/LCD display. Supports electronic array transducers (linear, curved, sector/phased, matrix, dual, CW, 3D). Connectivity via LAN/wireless. Complies with DICOM (NEMA PS 3.1-3.20). Biocompatible patient-contact materials. Safety standards: AAMI/ANSI ES60601-1, IEC 60601-1-2, IEC 60601-2-37, ISO 10993-1, IEC 62359.

Indications for Use

Indicated for ultrasound imaging, measurement, display, and analysis of human body and fluid in clinical applications including fetal/obstetrics, abdominal, pediatric, small organ, neonatal/adult cephalic, cardiac, peripheral vascular, musculoskeletal, urology, transvaginal/transrectal, and interventional guidance. For use by or under direction of qualified physicians in hospitals or private offices.

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.

Predicate Devices

• Vivid E95 (K200743)

Reference Devices

• Vivid S70N (K200497)
• NuVera Medical - NuVision ICE Catheter (K201775)

Submission Summary (Full Text)

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Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health and Human Services logo. To the right of that is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.

GE Medical Systems Ultrasound and Primary Care Diagnostics % Tracey Ortiz Regulatory Affairs Director 9900 W. Innovation Drive WAUWATOSA WI 53226

## Re: K202658

Trade/Device Name: Vivid E80/ Vivid E90/ Vivid E95 Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: Class II Product Code: IYN, IYO, ITX, OBJ Dated: February 12, 2021 Received: February 16, 2021

### Dear Tracey Ortiz:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and 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) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmp/pmn.cfm identifies combination product submissions. 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see

March 5, 2021

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https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.

For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email ([e-mail]) or phone [phone] or 301-796-7100).

Sincerely,

For

Thalia T. Mills, Ph.D. Director Division of Radiological Health OHT7: Office of In Vitro Diagnostics and Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health

Enclosure

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## Indications for Use

510(k) Number (if known)

#### K202658

Device Name

Vivid E80 / Vivid E90 / Vivid E95

#### Indications for Use (Describe)

Vivid E80 / Vivid E90 / Vivid E95 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified and trained physician for ultrasound imaging, measurement, display and analysis of the human body and fluid. The device is intended for use in a hospital environment including echo lab, other hospital settings, operating room, Cath lab and EP lab or in private medical offices. The systems support the following clinical applications: Fetal/Obstetrics, Abdominal (including renal, GYN), Pediatric, Small Organ (breast, testes, thyroid), Neonatal Cephalic, Cardiac (adult and pediatic), Peripheral Vascular, Musculo-sketal Conventional, Musculo-skeletal Superficial, Urology (including prostate), Transvaginal, Transvaginal, Transrectal, Interventional Guidance (including Biopsy, Vascular Access), Intra-cardiac, Intra-luminal and Intraoperative (vascular). Modes of operation include: 3D, Real time (RT) 3D Mode (4D), B, M, PW Doppler, CW Doppler, Color M Doppler, Power Doppler, Harmonic Imaging, Coded Pulse and Combined modes: B/M, B/Color M, B/PWD or CWD, B/Color/PWD or CWD, B/Power/PWD.

| Type of Use (Select one or both, as applicable) | |
|-------------------------------------------------------------------------------------------------------|---------------------------------------------|
| <span style="text-decoration: overline;"><b>X</b></span> Prescription Use (Part 21 CFR 801 Subpart D) | Over-The-Counter Use (21 CFR 801 Subpart C) |

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Image /page/3/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'G' and 'E' intertwined within a blue circle. The circle is surrounded by a stylized pattern of curved lines, also in blue, which gives the impression of motion or energy.

GE Healthcare 510(k) Premarket Notification Submission

| K202658 | 510(k) Summary |
|-------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Date:<br>Submitter: | In accordance with 21 CFR 807.92 the following summary of information is provided:<br>September 10, 2020<br>GE Medical Systems Ultrasound and Primary Care Diagnostics<br>9900 Innovation Drive<br>Wauwatosa, WI 53226 |
| Primary Contact Person: | Tracey Ortiz<br>Regulatory Affairs Director<br>GE Healthcare<br>T:[phone] |
| Secondary Contact Person: | Karim Amrouche<br>Regulatory Affairs Leader |
| Device Trade Name:<br>Common/Usual Name:<br>Classification Names: | Vivid E80 / Vivid E90 / Vivid E95<br>Diagnostic Ultrasound System<br>Class II |
| Product Code: | Ultrasonic Pulsed Doppler Imaging System. 21CFR 892.1550 90-<br>IYN; Ultrasonic Pulsed Echo Imaging System, 21CFR 892.1560,<br>90-IYO; Diagnostic Ultrasound Transducer, 21 CFR 892.1570,<br>90-ITX; Diagnostic intravascular catheter, 21 CFR 870.1200, 90-<br>OBJ |
| Primary Predicate Device:<br>Reference Device(s): | Vivid E95 (K200743)<br>Vivid S70N (K200497) |
| Device Description: | Vivid E80 / Vivid E90 / Vivid E95 is a Track 3, diagnostic<br>ultrasound system, which is primarily intended for cardiac<br>imaging and analysis but also includes vascular and general<br>radiology applications. It is a full featured diagnostic ultrasound<br>system that provides digital acquisition, processing, analysis and<br>display capability. |
| | The Vivid E80 / Vivid E90 / Vivid E95 consists of a mobile<br>console with a height-adjustable control panel, color LCD touch<br>panel, OLED or LCD display monitor (alternatives) and optional<br>image storage and printing devices. It includes a variety of<br>electronic array transducers operating in linear, curved, |

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sector/phased array, matrix array or dual array format, including dedicated CW transducers and real time 3D transducer.

The system includes electronics for transmit and receive of ultrasound data, ultrasound signal processing, software computing, hardware for Image storage, hard copy printing, and network access to the facility through both LAN and wireless (supported by use of a wireless LAN adapter) connection.

- Intended Use: Vivid E80 / Vivid E90 / Vivid E95 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified and trained physician for ultrasound imaging, measurement, display and analysis of the human body and fluid. The device is intended for use in a hospital environment including echo lab, other hospital settings, operating room, Cath lab and EP lab or in private medical offices. The systems support the following clinical applications: Fetal/Obstetrics, Abdominal (including renal, GYN), Pediatric, Small Organ (breast, testes, thyroid), Neonatal Cephalic, Adult Cephalic, Cardiac (adult and pediatric), Peripheral Vascular, Musculo-skeletal Conventional, Musculoskeletal Superficial, Urology (including prostate), Transesophageal, Transvaginal, Transrectal, Interventional Guidance (including Biopsy, Vascular Access), Intra-cardiac. Intra-luminal and Intraoperative (vascular). Modes of operation include: 3D, Real time (RT) 3D Mode (4D), B, M, PW Doppler, CW Doppler, Color Doppler, Color M Doppler, Power Doppler, Harmonic Imaging, Coded Pulse and Combined modes: B/M, B/Color M, B/PWD or CWD, B/Color/PWD or CWD, B/Power/PWD.
- The Vivid E80 / Vivid E90 / Vivid E95 employs the same Technology: fundamental scientific technology as its predicate devices.

Determination of Comparison to Predicate Devices Substantial Equivalence: The Vivid E80 / Vivid E90 / Vivid E95 is substantially equivalent to the predicate devices with regard to intended use, imaging capabilities, technological characteristics and safety and effectiveness.

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The following is an overview of the differences between the proposed Vivid E80 / Vivid E90 / Vivid E95 and its predicates. Indications for Use:

- Adding Intra-cardiac and Intra-luminal applications, . cleared in reference device Vivid S70N (K200497).
Features/Functionality:

- Adding an Authentication tool that will recognize the ICE ● catheter.
Transducers and Modes:

- . Adding an OEM ICE catheter (NuVera Medical -NuVision ICE Catheter, K201775) to the compatibile accessories list.
## Summary of Non-Clinical Tests:

Vivid E80 / Vivid E90 / Vivid E95 were evaluated for acoustic output, biocompatibility, cleaning and disinfection effectiveness as well as thermal, electrical, electromagnetic, and mechanical safety, and have been found to comply with applicable medical device safety standards. The Vivid E80 / Vivid E90 / Vivid E95 complies with voluntary standards:

- AAMI/ANSI ES60601-1, Medical Electrical Equipment -● Part 1: General Requirements for Safety and Essential Performance, 2005/ A2:2012
- IEC 60601-1-2, Medical Electrical Equipment Part 1-2: . General Requirements for Basic Safety and Essential Performance - Collateral Standard: Electromagnetic Disturbance - Requirements and Tests, 2014
- . IEC 60601-2-37, Medical Electrical Equipment - Part 2-37: Particular Requirements for the Safety of Ultrasonic Medical Diagnostic and Monitoring Equipment, 2015
- ISO 10993-1, Biological Evaluation of Medical Devices-. Part 1: Evaluation and Testing Within A Risk Management Process. 2009
- IEC 62359. Ultrasonics Field characterization Test ● methods for the determination of thermal and mechanical indices related to medical diagnostic ultrasonic fields, 2017

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Image /page/6/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'g' and 'e' intertwined in a stylized script, enclosed within a blue circle. The circle has a decorative border that resembles swirling lines or waves, giving the logo a classic and recognizable appearance.

# GE Healthcare

510(k) Premarket Notification Submission

- . ISO 14971, Application of risk management to medical devices, 2007
- . NEMA PS 3.1 - 3.20, Digital Imaging and Communication: in Medicine (DICOM) Set. (Radiology), 2016

The following quality assurance measures are applied to the development of the system:

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

Transducer material and other patient contact materials are biocompatible.

Summary of Clinical Tests:

The subject of this premarket submission, Vivid E80 /

Vivid E90 / Vivid E95, did not require clinical studies to support substantial equivalence.

- Conclusion: GE Healthcare considers the Vivid E80 / Vivid E90 / Vivid E95 to be as safe, as effective, and performance is substantially equivalent to the predicate and reference device.