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FDA 510(k)

一次性通用电极

K号: K152059 · 2016-04-21

决定日期2016-04-21
产品代码GEI
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

Disposable General Electrode is the device name listed in this FDA 510(k) record. The listed applicant is Modern Medical Equipment Manufacturing Limited. It received FDA 510(k) clearance on 2016-04-21 under 510(k) number K152059. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Disposable General Electrode?

Disposable General Electrode is a medical device that received FDA 510(k) clearance on 2016-04-21. The listed applicant is Modern Medical Equipment Manufacturing Limited. The 510(k) number is K152059.

When did Disposable General Electrode receive FDA 510(k) clearance?

Disposable General Electrode received FDA 510(k) clearance on 2016-04-21, under 510(k) number K152059.

Who is the listed applicant for Disposable General Electrode?

The FDA 510(k) record lists Modern Medical Equipment Manufacturing Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable General Electrode?

The FDA product code for Disposable General Electrode is GEI.

相关临床试验

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列明Modern Medical Equipment Manufacturing Limited为申报人的其他记录

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相关器械(代码:GEI)

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。

官方来源

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