ClearanceBrief
510(k) K221353 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Quantum Perfusion Dual Lumen Cannula 31F, Quantum Perfusion Dual Lumen Cannula 27F, Quantum Perfusion Dual Lumen Cannula 24F, Quantum Perfusion Dual Lumen Cannula 29F, Quantum Perfusion Dual Lumen Cannula 24F-V1, Quantum Perfusion Dual Lumen Cannula 27F-V1, Quantum Perfusion Dual Lumen Cannula 29F-V

ApplicantQura S.R.L, Mirandola, IT
DecisionSubstantially Equivalent, Aug 18, 2022
ReceivedMay 10, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K221353

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.