ClearanceBrief
510(k) K831436 ยท DTB Permanent Pacemaker Electrode

UNIPOLAR ATRIAL J PACING LEAD MODEL 869

ApplicantPacesetter Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Jun 8, 1983
ReceivedMay 4, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831436

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.