ClearanceBrief
510(k) K954719 ยท DTB Permanent Pacemaker Electrode

INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD

ApplicantIntermedics, Inc., Angleton TX, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Feb 27, 1996
ReceivedOct 13, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954719

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.