Submission Details
| 510(k) Number | K061330 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 12, 2006 |
| Decision Date | May 25, 2006 |
| Days to Decision | 13 days |
| Submission Type | Abbreviated |
| Review Panel | Ophthalmic (OP) |
| Summary | Statement |