ClearanceBrief
510(k) K862276 ยท DTB Permanent Pacemaker Electrode

MODEL 435-02 CARDIFIX IMPLANTABLE PACING LEAD

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Jul 2, 1986
ReceivedJun 16, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862276

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.