ClearanceBrief
510(k) K253376 · KRD Device, Vascular, For Promoting Embolization

OBSIDIO™ Conformable Embolic (M0013972101010)

ApplicantBoston Scientific Corporation, Maple Grove MN, US
DecisionSubstantially Equivalent, Oct 30, 2025
ReceivedSep 30, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K253376

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.