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FDA 510(k)

GE LOGIQ P6/P6 PRO

K-Number: K101874 · 2010-10-05

ApplicantGE Healthcare
Decision Date2010-10-05
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE LOGIQ P6/P6 PRO is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2010-10-05 under 510(k) number K101874. 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 P6/P6 PRO?

GE LOGIQ P6/P6 PRO is a medical device that received FDA 510(k) clearance on 2010-10-05. The listed applicant is GE Healthcare. The 510(k) number is K101874.

When did GE LOGIQ P6/P6 PRO receive FDA 510(k) clearance?

GE LOGIQ P6/P6 PRO received FDA 510(k) clearance on 2010-10-05, under 510(k) number K101874.

Who is the listed applicant for GE LOGIQ P6/P6 PRO?

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 P6/P6 PRO?

The FDA product code for GE LOGIQ P6/P6 PRO is IYN.

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Other records listing GE Healthcare as applicant

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Related Devices (Code: IYN)

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.

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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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