Alcon Universal, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alcon Universal, Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Alcon Universal, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Fort Worth, US.
Historical record: 5 cleared submissions from 2000 to 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Alcon Universal, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alcon Universal, Ltd.
5 devices
Cleared
Aug 08, 2002
OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION
Ophthalmic
121d
Cleared
Oct 23, 2000
OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION
Ophthalmic
63d
Cleared
Jul 10, 2000
OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION
Ophthalmic
87d
Cleared
Jul 03, 2000
OPTI-FREE SUPRACLENS DAILY POTEIN REMOVER / RGP MULTI-PURPOSE DISINFECTING...
Ophthalmic
77d
Cleared
Apr 28, 2000
OPTI-FREE EXPRESS LENS DROPS
Ophthalmic
81d