FDA 510(k)

LZI 尼古丁 II 酶联免疫测定

K号: K192299 · 2019-11-21

决定日期2019-11-21

产品代码MKU

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决定实质等同

器械摘要

LZI Cotinine II Enzyme Immunoassay is the device name listed in this FDA 510(k) record. The listed applicant is Lin-Zhi International, Inc.. It received FDA 510(k) clearance on 2019-11-21 under 510(k) number K192299. The device is classified under product code MKU. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LZI Cotinine II Enzyme Immunoassay?

LZI Cotinine II Enzyme Immunoassay is a medical device that received FDA 510(k) clearance on 2019-11-21. The listed applicant is Lin-Zhi International, Inc.. The 510(k) number is K192299.

When did LZI Cotinine II Enzyme Immunoassay receive FDA 510(k) clearance?

LZI Cotinine II Enzyme Immunoassay received FDA 510(k) clearance on 2019-11-21, under 510(k) number K192299.

Who is the listed applicant for LZI Cotinine II Enzyme Immunoassay?

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

What is the FDA product code for LZI Cotinine II Enzyme Immunoassay?

The FDA product code for LZI Cotinine II Enzyme Immunoassay is MKU.

列明Lin-Zhi International, 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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