ClearanceBrief
510(k) K063619 ยท KRD Device, Vascular, For Promoting Embolization

FLIPPER DETACHABLE EMBOLIZATION COILS

ApplicantCook, Inc., Bloomington IN, US
DecisionSubstantially Equivalent, Dec 20, 2006
ReceivedDec 5, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K063619

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.