ClearanceBrief
510(k) K860547 ยท DTB Permanent Pacemaker Electrode

MODEL 486-02 ENDOCARDIAL PACING LEAD

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Jun 13, 1986
ReceivedFeb 13, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860547

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.