ClearanceBrief
510(k) K790345 ยท GXY Electrode, Cutaneous

STIMTECH TENS ELECTRODE

ApplicantStimulation Technology, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 21, 1979
ReceivedFeb 21, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790345

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.