FDA 510(k)

GE LOGIQ 5 PRO OR EXPERT

K-Number: K032974 · 2003-10-21

Decision Date2003-10-21

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 5 PRO OR EXPERT is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 2003-10-21 under 510(k) number K032974. 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 5 PRO OR EXPERT?

GE LOGIQ 5 PRO OR EXPERT is a medical device that received FDA 510(k) clearance on 2003-10-21. The listed applicant is General Electric Co.. The 510(k) number is K032974.

When did GE LOGIQ 5 PRO OR EXPERT receive FDA 510(k) clearance?

GE LOGIQ 5 PRO OR EXPERT received FDA 510(k) clearance on 2003-10-21, under 510(k) number K032974.

Who is the listed applicant for GE LOGIQ 5 PRO OR EXPERT?

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

What is the FDA product code for GE LOGIQ 5 PRO OR EXPERT?

The FDA product code for GE LOGIQ 5 PRO OR EXPERT is IYN.

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Other records listing General Electric Co. as applicant

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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.