ClearanceBrief
510(k) K904113 ยท IKO Hammer, Reflex, Powered

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ApplicantMedical Dynamics, Inc., Englewood CO, US
DecisionSubstantially Equivalent, Oct 30, 1990
ReceivedSep 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904113

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.