FDA 510(k)

GE LOGIQ 9 MODEL 2375600

K-Number: K030934 · 2003-04-17

Decision Date2003-04-17

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 9 MODEL 2375600 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, Inc.. It received FDA 510(k) clearance on 2003-04-17 under 510(k) number K030934. 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 9 MODEL 2375600?

GE LOGIQ 9 MODEL 2375600 is a medical device that received FDA 510(k) clearance on 2003-04-17. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K030934.

When did GE LOGIQ 9 MODEL 2375600 receive FDA 510(k) clearance?

GE LOGIQ 9 MODEL 2375600 received FDA 510(k) clearance on 2003-04-17, under 510(k) number K030934.

Who is the listed applicant for GE LOGIQ 9 MODEL 2375600?

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

What is the FDA product code for GE LOGIQ 9 MODEL 2375600?

The FDA product code for GE LOGIQ 9 MODEL 2375600 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.