Medical Device Manufacturer · US , Cleveland , TN

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

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Unicor, Inc. has 5 FDA 510(k) cleared medical devices. Based in Cleveland, US.

Historical record: 5 cleared submissions from 1995 to 1995. Primary specialty: Anesthesiology.

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

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

5 devices

1-5 of 5