ClearanceBrief
510(k) K993677 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT

ApplicantMedtronic Vascular, Grand Rapids MI, US
DecisionSubstantially Equivalent, Apr 17, 2000
ReceivedNov 1, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993677

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.