ClearanceBrief
510(k) K875048 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

SARNS VENOATRIAL CATHETER

Applicant3M Health Care, Sarns, Ann Arbor MI, US
DecisionSubstantially Equivalent, Feb 18, 1988
ReceivedDec 9, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875048

DateFirm and productCodeLinked 510(k)
Jul 23, 2014Terumo Cardiovascular Systems Corporation
Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These
Terminated
DWFNone listed

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