ClearanceBrief
510(k) K061565 ยท DQO Catheter, Intravascular, Diagnostic

LANGSTON DUAL LUMEN CATHETER

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 2, 2006
ReceivedJun 5, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061565

DateFirm and productCodeLinked 510(k)
Oct 20, 2020Vascular Solutions, Inc.
Langston Dual Lumen Catheter.
Terminated
DQONone listed
Jul 11, 2011Vascular Solutions, Inc.
Langston Dual Lumen Catheters, REF 5515, 7F, Sterile EO, Rx ONLY, 1 x Catheter and 5 x Catheter, Vascular Solutions, Inc., 6464 Sycamore Court, Minneapolis, MN 55369. Langston dual lumen catheters a
Terminated
DQONone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.