ClearanceBrief
510(k) K053444 ยท HKX Tonometer, Ac-Powered

KOWA KT-800

ApplicantKowa Co. , Ltd., Mie-Ken, JP
DecisionSubstantially Equivalent, Jun 9, 2006
ReceivedDec 9, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053444

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.