FDA 510(k)

Lumipulse G ROMA

K号: K160090 · 2016-05-16

决定日期2016-05-16

产品代码ONX

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决定实质等同

器械摘要

Lumipulse G ROMA 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 2016-05-16 under 510(k) number K160090. The device is classified under product code ONX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Lumipulse G ROMA?

Lumipulse G ROMA is a medical device that received FDA 510(k) clearance on 2016-05-16. The listed applicant is Fujirebio Diagnostics,Inc.. The 510(k) number is K160090.

When did Lumipulse G ROMA receive FDA 510(k) clearance?

Lumipulse G ROMA received FDA 510(k) clearance on 2016-05-16, under 510(k) number K160090.

Who is the listed applicant for Lumipulse G ROMA?

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 ROMA?

The FDA product code for Lumipulse G ROMA is ONX.

列明Fujirebio Diagnostics,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。

K250925ADVIA Centaur 鳞状细胞癌相关抗原21-1 K242706Lumipulse G pTau217/β-淀粉样蛋白 1-42 血浆比值 K192524Lumipulse G CA15-3 K192380ST AIA-PACK BNP K200997Lumipulse G CA19-9-N K190702Lumipulse G 全部 PTH

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