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FDA 510(k)

FLEX 微波消融系统及其附件

K号: K163118 · 2017-03-09

决定日期2017-03-09
产品代码NEY
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。
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器械摘要

FLEX Microwave Ablation System and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Neuwave Medical, Inc.. It received FDA 510(k) clearance on 2017-03-09 under 510(k) number K163118. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FLEX Microwave Ablation System and Accessories?

FLEX Microwave Ablation System and Accessories is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Neuwave Medical, Inc.. The 510(k) number is K163118.

When did FLEX Microwave Ablation System and Accessories receive FDA 510(k) clearance?

FLEX Microwave Ablation System and Accessories received FDA 510(k) clearance on 2017-03-09, under 510(k) number K163118.

Who is the listed applicant for FLEX Microwave Ablation System and Accessories?

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

What is the FDA product code for FLEX Microwave Ablation System and Accessories?

The FDA product code for FLEX Microwave Ablation System and Accessories is NEY.

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列明Neuwave Medical, Inc.为申报人的其他记录

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相关器械(代码:NEY)

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。

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