ClearanceBrief
510(k) K874167 ยท DTB Permanent Pacemaker Electrode

MEDTRONIC PERMANENT LEAD INTRODUCER

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Dec 7, 1987
ReceivedOct 13, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874167

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.