Medical Device Manufacturer · US , Van Nuys , CA

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

4 submissions · 4 cleared · Since 1991

Total

Cleared

Denied

Somnitec, Inc. has 4 FDA 510(k) cleared medical devices. Based in Van Nuys, US.

Historical record: 4 cleared submissions from 1991 to 1991. Primary specialty: Neurology.

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

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

4 devices

1-4 of 4