ClearanceBrief
510(k) K951737 ยท FOS Catheter, Umbilical Artery

ARGYLE NEO-SERT TRIPLE LUMEN UMBILICAL VESSEL CATHETER INSERTION TRAY

ApplicantSherwood Medical Co., St. Louis MO, US
DecisionSubstantially Equivalent, Sep 28, 1995
ReceivedApr 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951737

DateFirm and productCodeLinked 510(k)
May 29, 2025Cardinal Health 200, LLC
Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs
Open, Classified
FOSNone listed

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