ClearanceBrief
510(k) K032542 ยท HCG Device, Neurovascular Embolization

MODIFICATION TO CONTOUR SE MICROSPHERES

ApplicantBoston Scientific Corp, Glens Falls NY, US
DecisionSubstantially Equivalent, Sep 16, 2003
ReceivedAug 18, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032542

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.