ClearanceBrief
510(k) K013805 ยท HKX Tonometer, Ac-Powered

KOWA AUTOMATED TONOMETER KT-500

ApplicantKowa Optimed, Inc., Washington DC, US
DecisionSubstantially Equivalent, Oct 11, 2002
ReceivedNov 15, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013805

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.