ClearanceBrief
510(k) K220866 ยท QEY Mechanical Thrombolysis Catheter

EKOS+ Endovascular Device

ApplicantBoston Scientific, Maple Grove MN, US
DecisionSubstantially Equivalent, Apr 20, 2022
ReceivedMar 25, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K220866

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.