Medical Device Manufacturer · US , Ames , IA

Full Spectrum, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1996

Total

Cleared

Denied

Full Spectrum, Inc. has 3 FDA 510(k) cleared medical devices. Based in Ames, US.

Historical record: 3 cleared submissions from 1996 to 1997. Primary specialty: General & Plastic Surgery.

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

Full Spectrum, Inc. is one of 12870 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Full Spectrum, Inc.

3 devices

1-3 of 3