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FDA 510(k)

一次性医用乳胶检查手套(LG100)

K号: K222693 · 2022-09-24

决定日期2022-09-24
产品代码LYY
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

Single-use medical latex examination gloves (LG100) is the device name listed in this FDA 510(k) record. The listed applicant is Fitone Latex Products Co., Ltd. Guangdong. It received FDA 510(k) clearance on 2022-09-24 under 510(k) number K222693. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Single-use medical latex examination gloves (LG100)?

Single-use medical latex examination gloves (LG100) is a medical device that received FDA 510(k) clearance on 2022-09-24. The listed applicant is Fitone Latex Products Co., Ltd. Guangdong. The 510(k) number is K222693.

When did Single-use medical latex examination gloves (LG100) receive FDA 510(k) clearance?

Single-use medical latex examination gloves (LG100) received FDA 510(k) clearance on 2022-09-24, under 510(k) number K222693.

Who is the listed applicant for Single-use medical latex examination gloves (LG100)?

The FDA 510(k) record lists Fitone Latex Products Co., Ltd. Guangdong as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Single-use medical latex examination gloves (LG100)?

The FDA product code for Single-use medical latex examination gloves (LG100) is LYY.

相关临床试验

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列明Fitone Latex Products Co., Ltd. Guangdong为申报人的其他记录

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相关器械(代码:LYY)

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官方来源

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