ClearanceBrief
510(k) K034068 ยท KRD Device, Vascular, For Promoting Embolization

CONTOUR SE MICROSPHERES

ApplicantBoston Scientific Corp, Natick, MA, US
DecisionSubstantially Equivalent, Mar 26, 2004
ReceivedDec 31, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K034068

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.