FDA 510(k)

GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION

K-Number: K993364 · 1999-11-05

Decision Date1999-11-05

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION 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 1999-11-05 under 510(k) number K993364. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION?

GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION is a medical device that received FDA 510(k) clearance on 1999-11-05. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K993364.

When did GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION receive FDA 510(k) clearance?

GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION received FDA 510(k) clearance on 1999-11-05, under 510(k) number K993364.

Who is the listed applicant for GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION?

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 700 WITH CODED EXCITATION MODIFICATION?

The FDA product code for GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION is IYO.

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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.