510(k) K895196 ยท HQF Laser, Ophthalmic
MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR
| Applicant | Nidek, Inc., El Toro CA, US |
| Decision | Substantially Equivalent, Oct 16, 1989 |
| Received | Aug 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895196
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.