ClearanceBrief
510(k) K912235 ยท DTB Permanent Pacemaker Electrode

MODELS 432-03 & 433-03 IMPLANT ENDOCARD PAC LEAD

ApplicantIntermedics, Inc., Freeport TX, US
DecisionSubstantially Equivalent, Sep 18, 1991
ReceivedMay 14, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912235

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.