Source document or public record
FDA 510(k) K232434 — BD Veritor System for Rapid Detection of Flu A+B CLIA Waived Kit
FDA 510(k) index record K232434. Device: BD Veritor System for Rapid Detection of Flu A+B CLIA Waived Kit. Applicant as listed: Bd. Decision date: 2023-12-05.
Source
"device_name": "BD Veritor System for Rapid Detection of Flu A+B CLIA Waived Kit"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K232434.
Device name: BD Veritor System for Rapid Detection of Flu A+B CLIA Waived Kit. Applicant as listed: Bd.
Decision date: 2023-12-05. Decision wording: Substantially Equivalent.
Product code: PSZ. Regulation: 21 CFR 866.3328. 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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