ClearanceBrief
510(k) K050168 ยท DQO Catheter, Intravascular, Diagnostic

LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, May 18, 2005
ReceivedJan 26, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050168

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.