Medical Device Manufacturer · US , Buffalo , NY

Safetec of America, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1995

Total

Cleared

Denied

Safetec of America, Inc. has 3 FDA 510(k) cleared medical devices. Based in Buffalo, US.

Historical record: 3 cleared submissions from 1995 to 1996. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Safetec of America, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Safetec of America, Inc.

4 devices

1-4 of 4