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FDA 510(k)

GORE VIABIL 短导丝胆道支架

K号: K170740 · 2017-05-08

决定日期2017-05-08
产品代码FGE
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定Unknown

器械摘要

GORE VIABIL Short Wire Biliary Endoprosthesis is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 2017-05-08 under 510(k) number K170740. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常见问题

What is the GORE VIABIL Short Wire Biliary Endoprosthesis?

GORE VIABIL Short Wire Biliary Endoprosthesis is a medical device that received FDA 510(k) clearance on 2017-05-08. The listed applicant is W. L. Gore & Associates, Inc.. The 510(k) number is K170740.

When did GORE VIABIL Short Wire Biliary Endoprosthesis receive FDA 510(k) clearance?

GORE VIABIL Short Wire Biliary Endoprosthesis received FDA 510(k) clearance on 2017-05-08, under 510(k) number K170740.

Who is the listed applicant for GORE VIABIL Short Wire Biliary Endoprosthesis?

The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GORE VIABIL Short Wire Biliary Endoprosthesis?

The FDA product code for GORE VIABIL Short Wire Biliary Endoprosthesis is FGE.

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列明W. L. Gore & Associates, Inc.为申报人的其他记录

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相关器械(代码:FGE)

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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