S & T AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
S & T AG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
S & T AG has 2 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by S & T AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - S & T AG
2 devices