ClearanceBrief
510(k) K032613 ยท LDF Electrode, Pacemaker, Temporary

TEMPORARY TRANSVENOUS PACEMAKER PLACEMENT ASSIST DEVICE

ApplicantPeter M. Rothenberg, M.D., San Clemente CA, US
DecisionSubstantially Equivalent, Nov 20, 2003
ReceivedAug 25, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032613

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.