FDA applicant
Becton Dickinson Vascular Access, Inc.
FDA records 25 decisions for Becton Dickinson Vascular Access, Inc. (Sandy, UT) from 1992 to 1997: 25 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and FPA (Set, Administration, Intravascular). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Becton Dickinson Vascular Access, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Becton Dickinson Vascular Access, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Becton Dickinson Vascular Access, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Becton”
FDA records each applicant name separately; these may or may not be the same firm.