ClearanceBrief
510(k) K781498 ยท DTB Permanent Pacemaker Electrode

LIFELINE BIPOLAR PACING LEAD MOD. 466-01

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

Recalls that name K781498

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.