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FDA 510(k)

Hevylite 人 IgG Kappa 套件用于 SPAPLUS，Hevylite 人 IgG Lambda 套件用于 SPAPLUS

K号: K161854 · 2016-10-04

申请人The Binding Site Group , Ltd.
决定日期2016-10-04
产品代码PCN
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决定实质等同

器械摘要

Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS is the device name listed in this FDA 510(k) record. The listed applicant is The Binding Site Group , Ltd.. It received FDA 510(k) clearance on 2016-10-04 under 510(k) number K161854. The device is classified under product code PCN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS?

Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS is a medical device that received FDA 510(k) clearance on 2016-10-04. The listed applicant is The Binding Site Group , Ltd.. The 510(k) number is K161854.

When did Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS receive FDA 510(k) clearance?

Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS received FDA 510(k) clearance on 2016-10-04, under 510(k) number K161854.

Who is the listed applicant for Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS?

The FDA 510(k) record lists The Binding Site Group , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS?

The FDA product code for Hevylite Human IgG Kappa Kit for use on the SPAPLUS, Hevylite Human IgG Lambda Kit for use on the SPAPLUS is PCN.

相关临床试验

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明The Binding Site Group , Ltd.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。

K250159免疫球蛋白同种型（GAM）用于EXENT分析器；EXENT分析器K250549Optilite® Freelite Mx Kappa Free Kit；Optilite® Freelite Mx Lambda Free KitK192116Human IgA 液体试剂套件用于 SPAPlusK191985Optilite IgA KitK191635Optilite IgM KitK191465Human IgM 套件用于 SPAPlus

查看所有 17 个设备 →

相关器械（代码：PCN）

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。

K172613Optilite Hevylite IgG Kappa Kit，Optilite Hevylite IgG Lambda KitThe Binding Site Group , Ltd.

官方来源

在 FDA 数据库中查看 →

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