Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W)
K号: K243030 · 2024-10-25
广告
器械摘要
常见问题
What is the Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W)?
Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) is a medical device that received FDA 510(k) clearance on 2024-10-25. The listed applicant is Ulike Co., Ltd.. The 510(k) number is K243030.
When did Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) receive FDA 510(k) clearance?
Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) received FDA 510(k) clearance on 2024-10-25, under 510(k) number K243030.
Who is the listed applicant for Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W)?
The FDA 510(k) record lists Ulike Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W)?
The FDA product code for Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W) is OHT.
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Ulike 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：OHT）
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。
广告