ClearanceBrief
510(k) K190594 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

AngioVac C20, AngioVac C180

ApplicantAngioDynamics, Inc., Marlborough MA, US
DecisionSubstantially Equivalent, Jul 5, 2019
ReceivedMar 7, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190594

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.