510(k) K902500 ยท HKO Refractometer, Ophthalmic
AR-1600G AUTO-REFRACTOMETER
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jul 27, 1990 |
| Received | Jun 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902500
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.