510(k) K062369 ยท GEX Powered Laser Surgical Instrument
IRIDEX OCULIGHT TX
| Applicant | Iridex Corp, Mountain View CA, US |
| Decision | Substantially Equivalent, Nov 8, 2006 |
| Received | Aug 14, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062369
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.