K243872
- 510(k) number
- K243872
- Device name
- BD Veritor System for SARS-CoV-2
- Applicant
- Becton, Dickinson and Company MD · US
- Product code
- QVF — Simple Point-Of-Care Device To Directly Detect Sars-
- Decision date
- 2025-06-16
- Date received
- 2024-12-17
- Decision
- Substantially Equivalent
- Clearance type
- Dual Track
- Advisory committee
- Microbiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K243872.pdf
Official FDA record: K243872
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.