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FDA 510(k)

LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3

K-Number: K161224 · 2016-08-05

ApplicantGE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Decision Date2016-08-05
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 is a medical device manufactured by GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC. It received FDA 510(k) clearance on 2016-08-05 under approval number K161224. 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 LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3?

LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 is a medical device that received FDA 510(k) clearance on 2016-08-05. It is manufactured by GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC. The 510(k) number is K161224.

When was LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 approved by the FDA?

LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 received FDA 510(k) clearance on 2016-08-05, under approval number K161224.

What company makes LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3?

LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 is manufactured by GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC.

What is the FDA product code for LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3?

The FDA product code for LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3 is IYN.

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Related Devices (Code: IYN)

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Official Source

View on FDA Database →

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

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