ClearanceBrief
510(k) K140999 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

TANDEMHEART VENO-VENOUS CANNULA

ApplicantCardiacassist, Inc., Pittsburgh PA, US
DecisionSubstantially Equivalent, Aug 6, 2014
ReceivedApr 18, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140999

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.