FDA 510(k)

BD 阴道面板

K号: K223653 · 2023-03-06

决定日期2023-03-06

产品代码PQA

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决定实质等同

器械摘要

BD Vaginal Panel 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 2023-03-06 under 510(k) number K223653. The device is classified under product code PQA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Vaginal Panel?

BD Vaginal Panel is a medical device that received FDA 510(k) clearance on 2023-03-06. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K223653.

When did BD Vaginal Panel receive FDA 510(k) clearance?

BD Vaginal Panel received FDA 510(k) clearance on 2023-03-06, under 510(k) number K223653.

Who is the listed applicant for BD Vaginal Panel?

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 Vaginal Panel?

The FDA product code for BD Vaginal Panel is PQA.

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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