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FDA 510(k)

Habib EUS RFA

K号: K161305 · 2016-07-07

决定日期2016-07-07
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

Habib EUS RFA is the device name listed in this FDA 510(k) record. The listed applicant is Emcision , Ltd.. It received FDA 510(k) clearance on 2016-07-07 under 510(k) number K161305. 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 Habib EUS RFA?

Habib EUS RFA is a medical device that received FDA 510(k) clearance on 2016-07-07. The listed applicant is Emcision , Ltd.. The 510(k) number is K161305.

When did Habib EUS RFA receive FDA 510(k) clearance?

Habib EUS RFA received FDA 510(k) clearance on 2016-07-07, under 510(k) number K161305.

Who is the listed applicant for Habib EUS RFA?

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

What is the FDA product code for Habib EUS RFA?

The FDA product code for Habib EUS RFA is GEI.

相关临床试验

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列明Emcision , Ltd.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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