510(k) K781965 ยท HQF Laser, Ophthalmic
LASER COAGULATOR, MODEL 41AK
| Applicant | Lasertek OY, Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 8, 1979 |
| Received | Nov 24, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781965
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.