ClearanceBrief
510(k) K220600 ยท QEW Peripheral Mechanical Thrombectomy With Aspiration

Artix Thrombectomy Device

ApplicantInari Medical, Irvine CA, US
DecisionSubstantially Equivalent, Mar 25, 2022
ReceivedMar 2, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K220600

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.