ClearanceBrief
510(k) K781499 ยท DTB Permanent Pacemaker Electrode

LIFELINE PACING LEAD MODEL 467-01

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 1, 1979
ReceivedAug 30, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781499

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.