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.

Kmi Diagnostics, Inc. 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 - Kmi Diagnostics, Inc.

6 devices

1-6 of 6