510(k) K782106 ยท HQF Laser, Ophthalmic
COAGULATOR, MODEL 40 AARGON
| Applicant | Lasertek OY, Walker MI, US |
| Decision | Substantially Equivalent, Feb 8, 1979 |
| Received | Dec 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782106
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.