ClearanceBrief
510(k) K082767 ยท HKI Camera, Ophthalmic, Ac-Powered

KOWA NONMYD ALPHA-DIII

ApplicantKowa Co. , Ltd., Chuo-Ku, Tokyo, JP
DecisionSubstantially Equivalent, Oct 21, 2008
ReceivedSep 22, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082767

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.