Medical Device Manufacturer · US , Indianapolos , IN

Rochdiag - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2001

Total

Cleared

Denied

Rochdiag has 3 FDA 510(k) cleared medical devices. Based in Indianapolos, US.

Historical record: 3 cleared submissions from 2001 to 2007. Primary specialty: Chemistry.

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

Rochdiag is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Rochdiag

3 devices

1-3 of 3