510(k) K964290 ยท HLQ Keratoscope, Ac-Powered
EYECHEK
| Applicant | Reichert Ophthalmic Instruments, Div. Leica, Inc., Depew NY, US |
| Decision | Substantially Equivalent, Jan 9, 1997 |
| Received | Oct 28, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964290
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.