ClearanceBrief
510(k) K930876 ยท DTB Permanent Pacemaker Electrode

SILICONE BIPOLAR LEAD MODELS 1136T, 1142T &1146T

ApplicantSiemens-Pacesetter, Inc., Sylmar CA, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Jun 15, 1994
ReceivedFeb 19, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930876

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.