Medical Device Manufacturer · US , Rockville , MD

Gary A. Gelbfish - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 1997

Total

Cleared

Denied

Gary A. Gelbfish has 0 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 0 cleared submissions from 1997 to 1997. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Gary A. Gelbfish Filter by specialty or product code using the sidebar.

Gary A. Gelbfish is one of 9813 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gary A. Gelbfish

1 devices

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