ClearanceBrief
510(k) K862765 ยท DRX Electrode, Electrocardiograph

EUROMED S-601

ApplicantLectec Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Aug 6, 1986
ReceivedJul 22, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862765

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.