ClearanceBrief
510(k) K862718 ยท GXY Electrode, Cutaneous

VERSA STIM

ApplicantConmedcorp, Utica NY, US
DecisionSubstantially Equivalent, Sep 9, 1986
ReceivedJul 17, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862718

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.