Medical Device Manufacturer · US , Meriden , CT

Canberra Industries, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1983

Total

Cleared

Denied

Canberra Industries, Inc. has 3 FDA 510(k) cleared medical devices. Based in Meriden, US.

Historical record: 3 cleared submissions from 1983 to 1993. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Canberra Industries, Inc.

3 devices

1-3 of 3