ClearanceBrief
510(k) K252569 ยท QJP Catheter, Percutaneous, Neurovasculature

Carrier XL Delivery Catheter

ApplicantBalt USA, LLC, Irvine CA, US
DecisionSubstantially Equivalent, Oct 22, 2025
ReceivedAug 14, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K252569

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.