510(k) K850665 ยท HLQ Keratoscope, Ac-Powered
CORNEASCOPE MODEL 1200
| Applicant | Kera Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Mar 20, 1985 |
| Received | Feb 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850665
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.