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FDA 510(k)

BD Veritor System for SARS-CoV-2

K-Number: K243872 · 2025-06-16

ApplicantBecton, Dickinson and Company
Decision Date2025-06-16
Product CodeQVF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD Veritor System for SARS-CoV-2 is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-06-16 under approval number K243872. The device is classified under product code QVF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Veritor System for SARS-CoV-2?

BD Veritor System for SARS-CoV-2 is a medical device that received FDA 510(k) clearance on 2025-06-16. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K243872.

When was BD Veritor System for SARS-CoV-2 approved by the FDA?

BD Veritor System for SARS-CoV-2 received FDA 510(k) clearance on 2025-06-16, under approval number K243872.

What company makes BD Veritor System for SARS-CoV-2?

BD Veritor System for SARS-CoV-2 is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Veritor System for SARS-CoV-2?

The FDA product code for BD Veritor System for SARS-CoV-2 is QVF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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