510(k) K801906 ยท HKO Refractometer, Ophthalmic
DIOPTRON III AUTOREFRACTOR
| Applicant | Coherent Medical Division, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 27, 1980 |
| Received | Aug 11, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801906
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.