ClearanceBrief
510(k) K893949 ยท KFK Saw, Pneumatically Powered

#157 EXAM LIGHT

ApplicantMedmark, Inc., Versailles OH, US
DecisionSubstantially Equivalent, Aug 7, 1989
ReceivedJun 1, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893949

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.