ClearanceBrief
510(k) K954780 ยท HKI Camera, Ophthalmic, Ac-Powered

KOWA PROFESSIONAL FUNDUS CAMERA MODELS FX-500, FX-500S, FX-500C

ApplicantKowa Optimed, Inc., Washington DC, US
DecisionSubstantially Equivalent, Dec 1, 1995
ReceivedOct 17, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954780

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.