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FDA 510(k)

Gammex PI泄漏检测无粉手术手套

K号: K171375 · 2018-02-06

决定日期2018-02-06
产品代码KGO
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

Gammex PI Breach Detect Powder Free Surgical Glove is the device name listed in this FDA 510(k) record. The listed applicant is Ansell Healthcare Products, LLC. It received FDA 510(k) clearance on 2018-02-06 under 510(k) number K171375. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Gammex PI Breach Detect Powder Free Surgical Glove?

Gammex PI Breach Detect Powder Free Surgical Glove is a medical device that received FDA 510(k) clearance on 2018-02-06. The listed applicant is Ansell Healthcare Products, LLC. The 510(k) number is K171375.

When did Gammex PI Breach Detect Powder Free Surgical Glove receive FDA 510(k) clearance?

Gammex PI Breach Detect Powder Free Surgical Glove received FDA 510(k) clearance on 2018-02-06, under 510(k) number K171375.

Who is the listed applicant for Gammex PI Breach Detect Powder Free Surgical Glove?

The FDA 510(k) record lists Ansell Healthcare Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Gammex PI Breach Detect Powder Free Surgical Glove?

The FDA product code for Gammex PI Breach Detect Powder Free Surgical Glove is KGO.

相关临床试验

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列明Ansell Healthcare Products, LLC为申报人的其他记录

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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相关器械(代码:KGO)

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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