ClearanceBrief
510(k) K854918 ยท DTB Permanent Pacemaker Electrode

MODEL 431-01 BIOPORE IMPLANTABLE PACING LEAD

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Mar 11, 1986
ReceivedDec 9, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854918

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.