Allergan Optical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allergan Optical - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Allergan Optical has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 1988 to 1988. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Allergan Optical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allergan Optical
2 devices