FDA applicant
B. Braun Vena-Tech
FDA records 2 decisions for B. Braun Vena-Tech (Evanston, IL) from 1992 to 1993: 2 510(k) clearances. All are in product code DTK (Filter, Intravascular, Cardiovascular). 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 B. Braun Vena-Tech’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for B. Braun Vena-Tech since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like B. Braun Vena-Tech’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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