FDA 510(k)

Elecsys TSH

K号: K190773 · 2019-04-16

决定日期2019-04-16

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

Elecsys TSH is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics. It received FDA 510(k) clearance on 2019-04-16 under 510(k) number K190773. 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 Elecsys TSH?

Elecsys TSH is a medical device that received FDA 510(k) clearance on 2019-04-16. The listed applicant is Roche Diagnostics. The 510(k) number is K190773.

When did Elecsys TSH receive FDA 510(k) clearance?

Elecsys TSH received FDA 510(k) clearance on 2019-04-16, under 510(k) number K190773.

Who is the listed applicant for Elecsys TSH?

FDA 510(k)记录显示罗氏诊断公司为申请人。这本身并不能确立该设备的制造商。

What is the FDA product code for Elecsys TSH?

The FDA product code for Elecsys TSH is JLW.

列明Roche Diagnostics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：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。

K251543Atellica® IM TSH3-Ultra II (TSH3ULII)Siemens Healthcare Diagnostics, Inc.K243570Dimension LOCI促甲状腺激素灵活试剂盒（TSHL）；Dimension LOCI游离甲状腺素灵活试剂盒（FT4L）Siemens Healthcare Diagnostics K234091Maverick诊断系统TC1000；Maverick测试面板A0.B0Genalyte, Inc.K233050ADVIA Centaur® TSH3-Ultra II (TSH3ULII)Siemens Healthcare Diagnostics, Inc.K222116Atellica® CI 分析仪, Atellica® IM 促甲状腺激素 3-Ultra (TSH3-UL), Atellica® CH 白蛋白BCP (AlbP)Siemens Healthcare Diagnostics, Inc.K221225Access TSH (3rd IS) 测定，DxI 9000 Access 免疫测定分析仪Beckman Coulter, Inc.

官方来源

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