Medical Device Manufacturer · US , San Leandro , CA

Allergan Humphrey - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1987

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Allergan Humphrey Ophthalmic ✕

2 devices

1-2 of 2

Cleared Jul 15, 1987

MODEL 3000 OPHTHALMIC SURGICAL SYSTEM

Ophthalmic · 92d

Cleared May 18, 1987

ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540

Ophthalmic · 38d