Medical Device Manufacturer · US , Plymouth , MN

Interrad Medical, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2008

Total

Cleared

Denied

Interrad Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Last cleared in 2021. Active since 2008. Primary specialty: General Hospital.

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

FDA 510(k) cleared devices by Interrad Medical, Inc.

7 devices

1-7 of 7