LUOFUCON® 硅胶银离子泡沫敷料, LUOFUCON® 硅胶银离子抗菌泡沫敷料
K号: K223360 · 2024-03-27
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器械摘要
常见问题
What is the LUOFUCON® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing?
LUOFUCON® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing is a medical device that received FDA 510(k) clearance on 2024-03-27. The listed applicant is Huizhou Foryou Medical Devices Co., Ltd.. The 510(k) number is K223360.
When did LUOFUCON® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing receive FDA 510(k) clearance?
LUOFUCON® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing received FDA 510(k) clearance on 2024-03-27, under 510(k) number K223360.
Who is the listed applicant for LUOFUCON® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam 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® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing?
The FDA product code for LUOFUCON® Silicone Ag+ Foam Dressing, LUOFUCON® Silicone Ag+ Antibacterial Foam Dressing is FRO. This falls under the Anesthesiology category.
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Huizhou Foryou Medical Devices 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:FRO)
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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