510(k) K031629 ยท HKI Camera, Ophthalmic, Ac-Powered
CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI
| Applicant | Canon USA, Inc., Lake Success NY, US |
| Decision | Substantially Equivalent, Jun 6, 2003 |
| Received | May 27, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031629
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.