Medical Device Manufacturer · US , San Leandro , CA

Allergan Humphrey - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1987

Total

Cleared

Denied

Allergan Humphrey has 3 FDA 510(k) cleared medical devices. Based in San Leandro, US.

Historical record: 3 cleared submissions from 1987 to 1990. Primary specialty: Ophthalmic.

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

FDA 510(k) Regulatory Record - Allergan Humphrey

3 devices

1-3 of 3