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FDA 510(k)

Bovie J-Plasma精确FLEX手柄

K号: K170777 · 2017-05-01

决定日期2017-05-01
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

Bovie J-Plasma Precise FLEX Handpiece is the device name listed in this FDA 510(k) record. The listed applicant is Bovie Medical Corporation. It received FDA 510(k) clearance on 2017-05-01 under 510(k) number K170777. 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 Bovie J-Plasma Precise FLEX Handpiece?

Bovie J-Plasma Precise FLEX Handpiece is a medical device that received FDA 510(k) clearance on 2017-05-01. The listed applicant is Bovie Medical Corporation. The 510(k) number is K170777.

When did Bovie J-Plasma Precise FLEX Handpiece receive FDA 510(k) clearance?

Bovie J-Plasma Precise FLEX Handpiece received FDA 510(k) clearance on 2017-05-01, under 510(k) number K170777.

Who is the listed applicant for Bovie J-Plasma Precise FLEX Handpiece?

The FDA 510(k) record lists Bovie Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bovie J-Plasma Precise FLEX Handpiece?

The FDA product code for Bovie J-Plasma Precise FLEX Handpiece is GEI.

相关临床试验

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列明Bovie Medical Corporation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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