510(k) K890559 ยท HKO Refractometer, Ophthalmic
NIDEK AR-1200
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Feb 27, 1989 |
| Received | Feb 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890559
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.