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FDA 510(k)

Lumipulse G TSH-III 免疫反应试剂盒

K号: K171103 · 2017-07-28

决定日期2017-07-28
产品代码JLW
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

Lumipulse G TSH-III Immunoreaction Cartridges is the device name listed in this FDA 510(k) record. The listed applicant is Fujirebio Diagnostics,Inc.. It received FDA 510(k) clearance on 2017-07-28 under 510(k) number K171103. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Lumipulse G TSH-III Immunoreaction Cartridges?

Lumipulse G TSH-III Immunoreaction Cartridges is a medical device that received FDA 510(k) clearance on 2017-07-28. The listed applicant is Fujirebio Diagnostics,Inc.. The 510(k) number is K171103.

When did Lumipulse G TSH-III Immunoreaction Cartridges receive FDA 510(k) clearance?

Lumipulse G TSH-III Immunoreaction Cartridges received FDA 510(k) clearance on 2017-07-28, under 510(k) number K171103.

Who is the listed applicant for Lumipulse G TSH-III Immunoreaction Cartridges?

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

What is the FDA product code for Lumipulse G TSH-III Immunoreaction Cartridges?

The FDA product code for Lumipulse G TSH-III Immunoreaction Cartridges is JLW.

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列明Fujirebio Diagnostics,Inc.为申报人的其他记录

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相关器械(代码:JLW)

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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