Medical Device Manufacturer · US , Minneapolis , MN

Kmi Diagnostics, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1997

Total

Cleared

Denied

Kmi Diagnostics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 6 cleared submissions from 1997 to 2002. Primary specialty: Chemistry.

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

6 devices

1–6 of 6