510(k) K954781 ยท HKI Camera, Ophthalmic, Ac-Powered
KOWA GENESIS HAND-HELD FUNDUS CAMERA
| Applicant | Kowa Optimed, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Dec 1, 1995 |
| Received | Oct 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954781
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.