ClearanceBrief
510(k) K091709 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

MULTI-MED CENTRAL VENOUS CATHETERS, MODELS: M3720HKIC, M4820HKIC

ApplicantEdwards Lifesciences, LLC, Irvine CA, US
DecisionSubstantially Equivalent, Oct 13, 2009
ReceivedJun 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091709

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.