510(k) K832089 ยท HQF Laser, Ophthalmic
MODEL 150K LASER COAGULATOR
| Applicant | Lasertek OY, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 30, 1984 |
| Received | Jun 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832089
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.