ClearanceBrief
510(k) K772357 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATORS

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Jan 17, 1978
ReceivedDec 27, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772357

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.