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FDA 510(k)

EUROIMMUN 抗西尼罗河病毒 ELISA(IgG)

K号: K153303 · 2016-08-10

决定日期2016-08-10
产品代码NOP
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器械摘要

EUROIMMUN Anti-West Nile Virus ELISA (IgG) is the device name listed in this FDA 510(k) record. The listed applicant is Euroimmun Us, Inc.. It received FDA 510(k) clearance on 2016-08-10 under 510(k) number K153303. The device is classified under product code NOP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EUROIMMUN Anti-West Nile Virus ELISA (IgG)?

EUROIMMUN Anti-West Nile Virus ELISA (IgG) is a medical device that received FDA 510(k) clearance on 2016-08-10. The listed applicant is Euroimmun Us, Inc.. The 510(k) number is K153303.

When did EUROIMMUN Anti-West Nile Virus ELISA (IgG) receive FDA 510(k) clearance?

EUROIMMUN Anti-West Nile Virus ELISA (IgG) received FDA 510(k) clearance on 2016-08-10, under 510(k) number K153303.

Who is the listed applicant for EUROIMMUN Anti-West Nile Virus ELISA (IgG)?

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

What is the FDA product code for EUROIMMUN Anti-West Nile Virus ELISA (IgG)?

The FDA product code for EUROIMMUN Anti-West Nile Virus ELISA (IgG) is NOP.

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列明Euroimmun Us, Inc.为申报人的其他记录

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相关器械(代码:NOP)

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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