510(k) K050562 ยท GEX Powered Laser Surgical Instrument
OCULIGHT GL/GLX
| Applicant | Iridex Corp, Mountain View CA, US |
| Decision | Substantially Equivalent, Apr 14, 2005 |
| Received | Mar 3, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050562
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.