ClearanceBrief
510(k) K871866 ยท DXY Implantable Pacemaker Pulse-Generator

MEDTRONIC CLASSIX MODELS 8436/8437/8438

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 10, 1987
ReceivedMay 13, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871866

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.