510(k) K882191 ยท HKO Refractometer, Ophthalmic
NIDEK ARK-2000
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jul 1, 1988 |
| Received | May 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882191
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.