ClearanceBrief
510(k) K062021 ยท HKI Camera, Ophthalmic, Ac-Powered

KOWA VX-10I

ApplicantKowa Co. , Ltd., Rockville MD, US
DecisionSubstantially Equivalent, Nov 1, 2006
ReceivedJul 17, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062021

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.