510(k) K960522 ยท HQF Laser, Ophthalmic
DIOPEXY PROBE
| Applicant | Iriderm Div., Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 19, 1996 |
| Received | Feb 6, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960522
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.