Medical Device Manufacturer · US , Lake Forest , IL

S & T AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

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.

S & T AG is one of 25284 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - S & T AG

2 devices

1-2 of 2