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FDA 510(k)

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel

K号: K214122 · 2022-07-28

决定日期2022-07-28
产品代码PCI
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决定实质等同

器械摘要

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial 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 2022-07-28 under 510(k) number K214122. The device is classified under product code PCI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel?

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K214122.

When did BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel receive FDA 510(k) clearance?

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel received FDA 510(k) clearance on 2022-07-28, under 510(k) number K214122.

Who is the listed applicant for BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial 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 MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel?

The FDA product code for BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel is PCI.

相关临床试验

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

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相关器械(代码:PCI)

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。

官方来源

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