510(k) K863591 ยท HQF Laser, Ophthalmic
ENDOPHOTOCOAGULATION PROBE
| Applicant | Mira, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Oct 10, 1986 |
| Received | Sep 15, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863591
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.