ClearanceBrief
510(k) K932892 ยท DTB Permanent Pacemaker Electrode

PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS

ApplicantSiemens-Pacesetter, Inc., Sylmar CA, US
DecisionUnknown, Jul 6, 1994
ReceivedJun 14, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932892

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.