510(k) K831083 ยท HKO Refractometer, Ophthalmic
AUTO REFRACTOMETER
| Applicant | Nidek, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 10, 1983 |
| Received | Apr 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831083
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.