FDA 510(k)

Vivid iq

K-Number: K200708 · 2020-09-09

ApplicantGe Medical Systems Ultrasound And

Decision Date2020-09-09

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Vivid iq is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Ultrasound And. It received FDA 510(k) clearance on 2020-09-09 under 510(k) number K200708. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vivid iq?

Vivid iq is a medical device that received FDA 510(k) clearance on 2020-09-09. The listed applicant is Ge Medical Systems Ultrasound And. The 510(k) number is K200708.

When did Vivid iq receive FDA 510(k) clearance?

Vivid iq received FDA 510(k) clearance on 2020-09-09, under 510(k) number K200708.

Who is the listed applicant for Vivid iq?

The FDA 510(k) record lists Ge Medical Systems Ultrasound And as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vivid iq?

The FDA product code for Vivid iq is IYN.

Other records listing Ge Medical Systems Ultrasound And as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K220882Vivid E80, Vivid E90, Vivid E95 K200743Vivid E80/ Vivid E90/ Vivid E95 K200138Versana Premier K192917ViewPoint 6

Related Devices (Code: IYN)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.