ClearanceBrief
510(k) K221470 ยท DQO Catheter, Intravascular, Diagnostic

Langston dual lumen catheter

ApplicantVascular Solutions, LLC, Minneapolis MN, US
DecisionSubstantially Equivalent, Jun 17, 2022
ReceivedMay 20, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K221470

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.