ClearanceBrief
510(k) K823831 ยท DXY Implantable Pacemaker Pulse-Generator

MEDTRONIC MODELS 59401 5941

ApplicantMedtronic Vascular, Mounds View MN, US
DecisionSubstantially Equivalent, Mar 16, 1983
ReceivedDec 21, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823831

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.