Medical Device Manufacturer · US , Walker , MI

Biotrine Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1981

Total

Cleared

Denied

Biotrine Corp. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 6 cleared submissions from 1981 to 1992. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Biotrine Corp.

6 devices

1-6 of 6