ClearanceBrief
510(k) K874735 ยท GXY Electrode, Cutaneous

DANTEC 13L35/36/37 STIM. AND RECORDING ELECTRODE

ApplicantDantec Electronics, Inc., Allendale NJ, US
DecisionSubstantially Equivalent, Jan 22, 1988
ReceivedNov 18, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874735

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.