ClearanceBrief
510(k) K830782 ยท DTB Permanent Pacemaker Electrode

LIFELINE ENDOCARDIAL PACING LEAD #479-05

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 18, 1983
ReceivedMar 11, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830782

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.