ClearanceBrief
510(k) K233824 ยท DYG Catheter, Flow Directed

Swan-Ganz catheter

ApplicantEdwards Lifesciences, LLC, Irvine CA, US
DecisionSubstantially Equivalent, Jun 6, 2024
ReceivedDec 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233824

DateFirm and productCodeLinked 510(k)
May 15, 2026Becton, Dickinson and Company
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
Open, Classified
DYBNone listed

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