ClearanceBrief
510(k) K912450 ยท DRX Electrode, Electrocardiograph

TRACETS SME 5000

ApplicantLectec Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Aug 28, 1991
ReceivedJun 3, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912450

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.