510(k) K861063 ยท HLQ Keratoscope, Ac-Powered
NIDEK KM-800 AUTO KERATOMETER
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Apr 4, 1986 |
| Received | Mar 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861063
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.