510(k) K101935 ยท HKI Camera, Ophthalmic, Ac-Powered
CENTERVUE DIGITAL RETINOGRAPHY SYSTEM
| Applicant | Centervue S.P.A., Rome, IT |
| Decision | Substantially Equivalent, Oct 27, 2010 |
| Received | Jul 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101935
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.