ClearanceBrief
510(k) K873931 ยท DTB Permanent Pacemaker Electrode

MODIFIED MODELS 1025M & 1026T PACING LEAD

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Oct 22, 1987
ReceivedSep 14, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873931

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.