510(k) K895474 ยท HKI Camera, Ophthalmic, Ac-Powered
NON-MYDRIATIC RETINAL CAMERA, CR4-45NM DUAL
| Applicant | Canon USA, Inc., Tokyo 146, JP |
| Decision | Substantially Equivalent, Oct 4, 1989 |
| Received | Sep 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895474
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.