ClearanceBrief
510(k) K234074 ยท QJP Catheter, Percutaneous, Neurovasculature

Next Generation Access Catheter

ApplicantBalt USA, LLC, Irvine CA, US
DecisionSubstantially Equivalent, Jul 2, 2024
ReceivedDec 22, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K234074

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.