Medical Device Manufacturer · US , Minneapolis , MN

Unipower Corp. - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 1994

Total

Cleared

Denied

Unipower Corp. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 1994 to 1994. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Unipower Corp.

3 devices

1-3 of 3