510(k) K812219 ยท HQF Laser, Ophthalmic
MODEL 900S INTRAOCULAR PROBE
| Applicant | Lumenis, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 16, 1981 |
| Received | Aug 6, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812219
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.