510(k) K895475 ยท HLQ Keratoscope, Ac-Powered
CANON AUTO REF-KERATOMETER RK-2
| Applicant | Canon USA, Inc., Tokyo 146, JP |
| Decision | Substantially Equivalent, Oct 31, 1989 |
| Received | Sep 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895475
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.