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FDA 510(k)

乙烯基手套

K号: K211904 · 2021-09-17

决定日期2021-09-17
产品代码LYZ
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Vinyl Glove is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Dihong Industry and Trade Co., Ltd.. It received FDA 510(k) clearance on 2021-09-17 under 510(k) number K211904. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Vinyl Glove?

Vinyl Glove is a medical device that received FDA 510(k) clearance on 2021-09-17. The listed applicant is Jiangsu Dihong Industry and Trade Co., Ltd.. The 510(k) number is K211904.

When did Vinyl Glove receive FDA 510(k) clearance?

Vinyl Glove received FDA 510(k) clearance on 2021-09-17, under 510(k) number K211904.

Who is the listed applicant for Vinyl Glove?

The FDA 510(k) record lists Jiangsu Dihong Industry and Trade Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vinyl Glove?

The FDA product code for Vinyl Glove is LYZ.

相关临床试验

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。

列明Jiangsu Dihong Industry and Trade Co., Ltd.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。

相关器械(代码:LYZ)

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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