Medical Device Manufacturer · US , Salt Lake City , UT

Fisma, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1996

Total

Cleared

Denied

Fisma, Inc. has 4 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Historical record: 4 cleared submissions from 1996 to 2000. Primary specialty: General & Plastic Surgery.

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

Fisma, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Fisma, Inc.

4 devices

1-4 of 4