ClearanceBrief
510(k) K080681 ยท HKI Camera, Ophthalmic, Ac-Powered

KOWA GENESIS-D

ApplicantKowa Co. , Ltd., Chuo-Ku, Tokyo, JP
DecisionSubstantially Equivalent, Apr 4, 2008
ReceivedMar 10, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080681

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.