ClearanceBrief
510(k) K961180 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

NMI ANTEGRAD CARDIOPLEGIA CANNULA

ApplicantNaltiac Medical, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Jun 21, 1996
ReceivedMar 26, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961180

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.