ClearanceBrief
510(k) K081560 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

VASCUTEK CANNULA GRAFT, MODEL CGS2008S

ApplicantVascutek, Ltd., Renfrewshire, Glasgow, GB
DecisionSubstantially Equivalent, Feb 10, 2009
ReceivedJun 3, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081560

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.