ClearanceBrief
510(k) K002578 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

AXILLARY ACCESS ARTERIAL CANNULA

ApplicantEdwards Lifesciences, LLC, Midvale UT, US
DecisionSubstantially Equivalent, Apr 11, 2002
ReceivedAug 18, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002578

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.