FDA 510(k)

BD Veritor System for SARS-CoV-2

K号: K243872 · 2025-06-16

决定日期2025-06-16

产品代码QVF

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决定实质等同

器械摘要

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

常见问题

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. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K243872.

When did BD Veritor System for SARS-CoV-2 receive FDA 510(k) clearance?

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

Who is the listed applicant for BD Veritor System for SARS-CoV-2?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

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.

列明Becton, Dickinson and Company为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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