510(k) K020374 ยท HQF Laser, Ophthalmic
OCULIGHT SL/SLX
| Applicant | Iridex Corp, Mountain View CA, US |
| Decision | Substantially Equivalent, May 3, 2002 |
| Received | Feb 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020374
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.