510(k) K862137 ยท HLQ Keratoscope, Ac-Powered
NIDEK KM-1000 SURGICAL KERATOMETER
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jul 23, 1986 |
| Received | Jun 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862137
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.