ClearanceBrief
510(k) K250283 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

RAP Femoral Venous Cannulae

ApplicantLivaNova USA, Inc., Arvada CO, US
DecisionSubstantially Equivalent, Jul 10, 2025
ReceivedJan 31, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K250283

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.