Medical Device Manufacturer · US , Hayward , CA

Cohort Medical Products Group, Inc. - FDA 510(k) Cleared Devices

5 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Cohort Medical Products Group, Inc. has 3 FDA 510(k) cleared medical devices. Based in Hayward, US.

Historical record: 3 cleared submissions from 1994 to 1997. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Cohort Medical Products Group, Inc.

5 devices

1-5 of 5