K963013 is an FDA 510(k) clearance for the PREFERENCE 60 AND PREFERENCE 60 TORIC. This device is classified as a Lenses, Soft Contact, Daily Wear (Class II - Special Controls, product code LPL).
Submitted by CooperVision, Inc. (Scottsville,, US). The FDA issued a Cleared decision on December 19, 1997, 507 days after receiving the submission on July 30, 1996.
This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.5925.
| 510(k) Number | K963013 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 30, 1996 |
| Decision Date | December 19, 1997 |
| Days to Decision | 507 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Statement |
| Product Code | LPL — Lenses, Soft Contact, Daily Wear |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 886.5925 |