ClearanceBrief
510(k) K973360 ยท LDF Electrode, Pacemaker, Temporary

MEDTRONIC MODEL 6416 TRANSVENOUS BIPOLAR TEMPORARY PACING LEAD

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, May 26, 1998
ReceivedSep 8, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973360

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.