Medical Device Manufacturer · US , Salt Lake City , UT

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

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

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

Historical record: 4 cleared submissions from 1988 to 1998. Primary specialty: Anesthesiology.

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

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

4 devices

1-4 of 4