ClearanceBrief
510(k) K853518 ยท DTB Permanent Pacemaker Electrode

LIFELINE ENDOCARDIAL BIPOLAR LEAD 476-06

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Nov 5, 1985
ReceivedAug 22, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853518

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.