FDA 510(k)

GE LOGIQ I, LOGIQ E AND VIVID E

K-Number: K113690 · 2011-12-29

Decision Date2011-12-29

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ I, LOGIQ E AND VIVID E is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2011-12-29 under 510(k) number K113690. 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 GE LOGIQ I, LOGIQ E AND VIVID E?

GE LOGIQ I, LOGIQ E AND VIVID E is a medical device that received FDA 510(k) clearance on 2011-12-29. The listed applicant is GE Healthcare. The 510(k) number is K113690.

When did GE LOGIQ I, LOGIQ E AND VIVID E receive FDA 510(k) clearance?

GE LOGIQ I, LOGIQ E AND VIVID E received FDA 510(k) clearance on 2011-12-29, under 510(k) number K113690.

Who is the listed applicant for GE LOGIQ I, LOGIQ E AND VIVID E?

The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GE LOGIQ I, LOGIQ E AND VIVID E?

The FDA product code for GE LOGIQ I, LOGIQ E AND VIVID E is IYN.

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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.