ClearanceBrief
510(k) K252213 ยท QJP Catheter, Percutaneous, Neurovasculature

Bendit17 Microcatheter

ApplicantBend IT Technologies, Ltd., Petach Tikva, IL
DecisionSubstantially Equivalent, Dec 3, 2025
ReceivedJul 15, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K252213

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.