510(k) K932836 ยท HQF Laser, Ophthalmic
NIDEK MODEL AC-2300
| Applicant | Nidek, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Nov 22, 1993 |
| Received | Jun 11, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932836
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.