ClearanceBrief
510(k) K955122 ยท DTB Permanent Pacemaker Electrode

INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD

ApplicantIntermedics, Inc., Angleton TX, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Nov 4, 1996
ReceivedNov 9, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955122

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.