ClearanceBrief
510(k) K925347 ยท DTB Permanent Pacemaker Electrode

MODEL 1148T TRANSVENOUS, SCREW-IN LEAD

ApplicantSiemens-Pacesetter, Inc., Sylmar CA, US
DecisionSubstantially Equivalent, Jun 10, 1993
ReceivedOct 22, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925347

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.