Medical Device Manufacturer · US , Sarasota , FL

Specs USA, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Specs USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sarasota, US.

Historical record: 2 cleared submissions from 1996 to 2000. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Specs USA, Inc.

2 devices

1-2 of 2