Documento fuente o registro público
FDA 510(k) K243872 — BD Veritor System for SARS-CoV-2
FDA 510(k) index record K243872. Device: BD Veritor System for SARS-CoV-2. Applicant as listed: Becton, Dickinson and Company. Decision date: 2025-06-16.
Fuente
"device_name": "BD Veritor System for SARS-CoV-2"
Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.
Review and references
Automated FDA record verification
2026-10-20
2026-10-24
professional use
FDA 510(k) public index record K243872.
Device name: BD Veritor System for SARS-CoV-2. Applicant as listed: Becton, Dickinson and Company.
Decision date: 2025-06-16. Decision wording: Substantially Equivalent.
Product code: QVF. Regulation: 21 CFR 866.3982. Medical specialty: Microbiology.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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