ClearanceBrief
510(k) K772202 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATOR, A-V SEQ.

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Dec 20, 1977
ReceivedNov 30, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772202

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.