FDA 510(k)

BD Vacutainer® 枸橼酸盐血液采集管

K号: K240455 · 2024-10-31

决定日期2024-10-31

产品代码GIM

咨询委员会CH 请注意，您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。

决定实质等同

器械摘要

BD Vacutainer® Citrate Blood Collection Tubes 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 2024-10-31 under 510(k) number K240455. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Vacutainer® Citrate Blood Collection Tubes?

BD Vacutainer® Citrate Blood Collection Tubes is a medical device that received FDA 510(k) clearance on 2024-10-31. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K240455.

When did BD Vacutainer® Citrate Blood Collection Tubes receive FDA 510(k) clearance?

BD Vacutainer® Citrate Blood Collection Tubes received FDA 510(k) clearance on 2024-10-31, under 510(k) number K240455.

Who is the listed applicant for BD Vacutainer® Citrate Blood Collection Tubes?

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 Vacutainer® Citrate Blood Collection Tubes?

The FDA product code for BD Vacutainer® Citrate Blood Collection Tubes is GIM.

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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官方来源

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