ClearanceBrief
510(k) K924642 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

MEDTRONIC BIO-MEDICUS FEMORAL CANNULA/INTRODUCER

ApplicantMedtronic Bio-Medicus, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Mar 26, 1993
ReceivedSep 14, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924642

DateFirm and productCodeLinked 510(k)
Jul 24, 2008Medtronic Perfusion Systems
Medtronic Bio-Medicus Femoral Cannula/Introducer, for Cardiopulmonary Bypass. Catalog Numbers: CB96345-023, CB96345-023, and CB96345-029.
Terminated
DWFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.