ClearanceBrief
510(k) K213589 ยท QJP Catheter, Percutaneous, Neurovasculature

FUBUKI XF Neurovascular Long Sheath

ApplicantAsahi Intecc Co., Ltd., Seto, JP
DecisionSubstantially Equivalent, Mar 24, 2022
ReceivedNov 12, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213589

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.