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.

510(k) submissions have been managed by Libramedical, Inc. as regulatory consultant.

Interrad Medical, 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 - Interrad Medical, Inc.

7 devices

1-7 of 7