Medical Device Manufacturer · US , Minneapolis , MN

Intervalve, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2013

Total

Cleared

Denied

Intervalve, Inc. has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 5 cleared submissions from 2013 to 2015. Primary specialty: Cardiovascular.

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

5 devices

1–5 of 5