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FDA 510(k)

LUOFUCON 胶原蛋白伤口敷料

K号: K213598 · 2022-09-20

决定日期2022-09-20
产品代码KGN
决定实质等同

器械摘要

LUOFUCON Collagen Wound Dressing is the device name listed in this FDA 510(k) record. The listed applicant is Huizhou Foryou Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2022-09-20 under 510(k) number K213598. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常见问题

What is the LUOFUCON Collagen Wound Dressing?

LUOFUCON Collagen Wound Dressing is a medical device that received FDA 510(k) clearance on 2022-09-20. The listed applicant is Huizhou Foryou Medical Devices Co., Ltd.. The 510(k) number is K213598.

When did LUOFUCON Collagen Wound Dressing receive FDA 510(k) clearance?

LUOFUCON Collagen Wound Dressing received FDA 510(k) clearance on 2022-09-20, under 510(k) number K213598.

Who is the listed applicant for LUOFUCON Collagen Wound Dressing?

FDA 510(k)记录将惠州友康医疗设备有限公司列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for LUOFUCON Collagen Wound Dressing?

The FDA product code for LUOFUCON Collagen Wound Dressing is KGN.

相关临床试验

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列明Huizhou Foryou Medical Devices Co., Ltd.为申报人的其他记录

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相关器械(代码:KGN)

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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