ClearanceBrief
510(k) K231393 ยท QJP Catheter, Percutaneous, Neurovasculature

Radical the Dude 7F Guide Catheter

ApplicantMaduro Medical, Inc., Campbell CA, US
DecisionSubstantially Equivalent, Nov 30, 2023
ReceivedMay 12, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231393

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.