Submission Details
| 510(k) Number | K943296 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 08, 1994 |
| Decision Date | September 14, 1994 |
| Days to Decision | 68 days |
| Submission Type | Traditional |
| Review Panel | Ophthalmic (OP) |
| Summary | Statement |
| Third-party Review | No - reviewed directly by FDA |