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.

A. Henniss 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 - A. Henniss

3 devices

1-3 of 3