Medical Device Manufacturer · US , San Jose , CA

Tetra Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1993

Total

Cleared

Denied

Tetra Corp. has 5 FDA 510(k) cleared medical devices. Based in San Jose, US.

Historical record: 5 cleared submissions from 1993 to 1996. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Tetra Corp.

5 devices

1-5 of 5