ClearanceBrief
510(k) K170544 ยท DQO Catheter, Intravascular, Diagnostic

Langston dual lumen catheter

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Nov 17, 2017
ReceivedFeb 24, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170544

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.