ClearanceBrief
510(k) K834134 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

SARNS 8.0 SOFT ARC CANNULA

Applicant3M Health Care, Sarns, Walker MI, US
DecisionSubstantially Equivalent, Apr 17, 1984
ReceivedNov 30, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834134

DateFirm and productCodeLinked 510(k)
Jul 23, 2014Terumo Cardiovascular Systems Corporation
Sarns Soft-arc Aortic Cannula 8.0mm curved tip, suture flange, 3/8" flare Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surg
Terminated
DWFNone listed

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