ClearanceBrief
510(k) K810734 ยท DXY Implantable Pacemaker Pulse-Generator

MODELS 8420 THRU 8423 PACEMAKER GENER

ApplicantMedtronic Vascular, Mounds View MN, US
DecisionSubstantially Equivalent, May 15, 1981
ReceivedMar 18, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810734

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.