Medical Device Manufacturer · US , Walker , MI

Centrimed Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1984

Total

Cleared

Denied

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

Historical record: 4 cleared submissions from 1984 to 1985. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Centrimed Corp.

4 devices

1-4 of 4