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

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.