Gsi Development Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gsi Development Co. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Gsi Development Co. has 4 FDA 510(k) cleared medical devices. Based in Carmel, US.
Historical record: 4 cleared submissions from 1988 to 1993. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Gsi Development Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gsi Development Co.
4 devices