ClearanceBrief
510(k) K150542 ยท DWE Tubing, Pump, Cardiopulmonary Bypass

Terumo Pump Tubing

ApplicantTerumo Cardiovascular Systems Corporation, Ashland MA, US
DecisionSubstantially Equivalent, May 1, 2015
ReceivedMar 3, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K150542

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.