Medical Device Manufacturer · US , Tarzana , CA

A. Henniss - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1990

Total

Cleared

Denied

A. Henniss has 3 FDA 510(k) cleared medical devices. Based in Tarzana, US.

Historical record: 3 cleared submissions from 1990 to 1991. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by A. Henniss Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - A. Henniss

3 devices

1-3 of 3