Allergan Medical Optics - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Allergan Medical Optics Ophthalmic ✕
7 devices
Cleared
Jun 15, 1995
AMO PROFINESSE III ULTRASONIC HANDPIECE SYSTEM
Ophthalmic
77d
Cleared
Jul 06, 1994
AMO PHACOFLEX INSERTER DISPOSABLE CARTRIDGE, AND HANDPIECE
Ophthalmic
96d
Cleared
Apr 07, 1994
AMO PHACOFLEX INSERTER, FOLDABLE IOL INSERT INSTR
Ophthalmic
440d
Cleared
Jan 07, 1993
AMO(R) FLRX-TIP(TM) DISPOS I/A HANDPIECE, OPO-38
Ophthalmic
80d
Cleared
Dec 23, 1992
AMO ELITE
Ophthalmic
121d
Cleared
Jul 26, 1991
MULTITOME MODEL 1000, VITRECTOMY DRIVING SYSTEM
Ophthalmic
88d
Cleared
Jun 16, 1989
PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR
Ophthalmic
51d