Medical Device Manufacturer · US , Costa Mesa , CA

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

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Intertherapy, Inc. has 5 FDA 510(k) cleared medical devices. Based in Costa Mesa, US.

Historical record: 5 cleared submissions from 1990 to 1991. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Intertherapy, Inc.

5 devices

1-5 of 5