510(k) K901009 ยท HLQ Keratoscope, Ac-Powered
MODEL 2000 INTRAOPERATIVE CORNEASCOPE
| Applicant | Kera Corp., Mountain View CA, US |
| Decision | Substantially Equivalent, May 30, 1990 |
| Received | Mar 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901009
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.