ClearanceBrief
510(k) K863366 ยท DRX Electrode, Electrocardiograph

PREGELLED DISPOS. ELECT., SILVER-SILVER CHLORIDE

ApplicantLabeltape Meditect, Inc., Grand Rapids MI, US
DecisionSubstantially Equivalent, Nov 21, 1986
ReceivedSep 3, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863366

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.