Submission Details
| 510(k) Number | K050157 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 25, 2005 |
| Decision Date | April 26, 2005 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
K050157 is an FDA 510(k) clearance for the MAXSIGHT (POLYMACON) SPORT-TINTED CONTACT LENS, a Lenses, Soft Contact, Daily Wear (Class II — Special Controls, product code LPL), submitted by Bausch & Lomb, Inc. (Rodchester, US). The FDA issued a Cleared decision on April 26, 2005, 91 days after receiving the submission on January 25, 2005. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.5925.
| 510(k) Number | K050157 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 25, 2005 |
| Decision Date | April 26, 2005 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Summary PDF |
| Product Code | LPL — Lenses, Soft Contact, Daily Wear |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 886.5925 |