ClearanceBrief
510(k) K133445 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

ANGIOVAC CANNULA

ApplicantVortex Medical, Inc., Marlborough MA, US
DecisionSubstantially Equivalent, Mar 5, 2014
ReceivedNov 12, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133445

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.