ClearanceBrief
510(k) K832124 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI

ApplicantMed-West, Inc., Walker MI, US
DecisionSubstantially Equivalent, Aug 12, 1983
ReceivedJun 30, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832124

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.