Company ยท US
Alcon Universal, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2002. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 8, 2002 | K021143 | OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION Alcon Universal, Ltd. | LPN |
| Oct 23, 2000 | K002589 | OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION Alcon Universal, Ltd. | LPN |
| Jul 10, 2000 | K001214 | OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION Alcon Universal, Ltd. | LPN |
| Jul 3, 2000 | K001235 | OPTI-FREE SUPRACLENS DAILY POTEIN REMOVER / RGP MULTI-PURPOSE DISINFECTING SOLUTION ID 100136 Alcon Universal, Ltd. | MRC |
| Apr 28, 2000 | K000385 | OPTI-FREE EXPRESS LENS DROPS Alcon Universal, Ltd. | MRC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||