ClearanceBrief
510(k) K822224 ยท GXY Electrode, Cutaneous

EMPI SINGLE USE

ApplicantEmpi, Walker MI, US
DecisionSubstantially Equivalent, Aug 16, 1982
ReceivedJul 27, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822224

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.