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FDA 510(k)

无粉乳胶检查手套,非无菌

K号: K221877 · 2022-07-23

决定日期2022-07-23
产品代码LZA
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

Powder-Free Nitrile Examination Glove, Non-Sterile is the device name listed in this FDA 510(k) record. The listed applicant is Goodgloves Industries Sdn Bhd. It received FDA 510(k) clearance on 2022-07-23 under 510(k) number K221877. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Powder-Free Nitrile Examination Glove, Non-Sterile?

Powder-Free Nitrile Examination Glove, Non-Sterile is a medical device that received FDA 510(k) clearance on 2022-07-23. The listed applicant is Goodgloves Industries Sdn Bhd. The 510(k) number is K221877.

When did Powder-Free Nitrile Examination Glove, Non-Sterile receive FDA 510(k) clearance?

Powder-Free Nitrile Examination Glove, Non-Sterile received FDA 510(k) clearance on 2022-07-23, under 510(k) number K221877.

Who is the listed applicant for Powder-Free Nitrile Examination Glove, Non-Sterile?

The FDA 510(k) record lists Goodgloves Industries Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Powder-Free Nitrile Examination Glove, Non-Sterile?

The FDA product code for Powder-Free Nitrile Examination Glove, Non-Sterile is LZA.

相关临床试验

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相关器械(代码:LZA)

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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