ClearanceBrief
510(k) K254223 ยท QJP Catheter, Percutaneous, Neurovasculature

Next Generation 088 Catheter

ApplicantBalt USA, LLC, Irvine CA, US
DecisionSubstantially Equivalent, Apr 16, 2026
ReceivedDec 29, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K254223

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.