Medical Device Manufacturer · US , Port Huron , MI

Biopro, Inc. - FDA 510(k) Cleared Devices

41 submissions · 35 cleared · Since 1987
41
Total
35
Cleared
0
Denied

Biopro, Inc. has 35 FDA 510(k) cleared medical devices. Based in Port Huron, US.

Historical record: 35 cleared submissions from 1987 to 2017.

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

FDA 510(k) cleared devices by Biopro, Inc.

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