510(k) K960971 ยท HQF Laser, Ophthalmic
OCULIGHT GL
| Applicant | Iriderm Div., Mountain View CA, US |
| Decision | Substantially Equivalent, Aug 28, 1996 |
| Received | Mar 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960971
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.