Gary A. Gelbfish is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gary A. Gelbfish - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
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.
FDA 510(k) Regulatory Record - Gary A. Gelbfish
1 devices