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FDA 510(k)

VITEK 2 AST-革兰氏阴性头孢唑啉(=<1-=>32 µg/mL)

K号: K251579 · 2025-08-21

决定日期2025-08-21
产品代码LON
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器械摘要

VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL) is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 2025-08-21 under 510(k) number K251579. The device is classified under product code LON. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)?

VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL) is a medical device that received FDA 510(k) clearance on 2025-08-21. The listed applicant is bioMerieux, Inc.. The 510(k) number is K251579.

When did VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL) receive FDA 510(k) clearance?

VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL) received FDA 510(k) clearance on 2025-08-21, under 510(k) number K251579.

Who is the listed applicant for VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)?

The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)?

The FDA product code for VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL) is LON.

相关临床试验

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列明bioMerieux, Inc.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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相关器械(代码:LON)

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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