510(k) K935747 ยท HQF Laser, Ophthalmic
MEGABEAM ENDOCULAR PROBE
| Applicant | Ceram Optec, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Apr 1, 1994 |
| Received | Dec 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935747
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.