ClearanceBrief
510(k) K961717 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

NMI RETROGRADE CARDIOPLEGIA CANNULA-RCCS

ApplicantNaltiac Medical, Inc., Dallas TX, US
DecisionSubstantially Equivalent, Jul 18, 1996
ReceivedMay 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961717

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.