Medical Device Manufacturer · US , Englewood , CO

Tetrad Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

Total

Cleared

Denied

Tetrad Corp. has 4 FDA 510(k) cleared medical devices. Based in Englewood, US.

Historical record: 4 cleared submissions from 2001 to 2004. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Tetrad Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tetrad Corp.

4 devices

1-4 of 4