Alcon Laboratories - FDA 510(k) Cleared Devices
47
Total
47
Cleared
0
Denied
FDA 510(k) Regulatory Record - Alcon Laboratories Ophthalmic ✕
35 devices
Cleared
Nov 05, 2007
NEXT GENERATION LASER
Ophthalmic
426d
Cleared
Apr 11, 2000
RGP MULTI-PURPOSE SOLUTION ID 100136
Ophthalmic
84d
Cleared
Sep 16, 1999
OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP
Ophthalmic
267d
Cleared
May 10, 1999
OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER
Ophthalmic
83d
Cleared
Jan 14, 1999
MULTI-PURPOSE DISINFECTING SOLUTION ID 90746
Ophthalmic
22d
Cleared
Dec 18, 1998
MULTI-PURPOSE DISINFECTING SOLUTION ID 90746
Ophthalmic
52d
Cleared
Dec 18, 1998
OPTI-ONE MULTI-PURPOSE SOLUTION
Ophthalmic
39d
Cleared
Jul 24, 1998
LIQUID ENZYME ID 90133
Ophthalmic
84d
Cleared
Jul 09, 1998
MONARCH IOL DELIVERY SYSTEM
Ophthalmic
66d
Cleared
Jun 23, 1998
TURBOSONICS LIMITED REUSE ULTRASONIC TIP
Ophthalmic
89d
Cleared
Jun 22, 1998
OPTI-FREE SUPRACLENS DAILY PROTEIN REMOVER/ALCON WETTING, SOAKING,...
Ophthalmic
84d
Cleared
May 19, 1998
CATARACT LIQUEFRACTURE DEVICE
Ophthalmic
113d