ClearanceBrief
510(k) K862257 ยท DTB Permanent Pacemaker Electrode

MODEL 431-02 BIOPORE IMPLANTABLE PACING LEAD

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Jul 10, 1986
ReceivedJun 13, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862257

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.