Trinity Plus 纹纹减少器
K号: K212947 · 2022-04-02
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决定日期2022-04-02
产品代码OHS
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Trinity Plus Wrinkle Reducer is the device name listed in this FDA 510(k) record. The listed applicant is Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2022-04-02 under 510(k) number K212947. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Trinity Plus Wrinkle Reducer?
Trinity Plus Wrinkle Reducer is a medical device that received FDA 510(k) clearance on 2022-04-02. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K212947.
When did Trinity Plus Wrinkle Reducer receive FDA 510(k) clearance?
Trinity Plus Wrinkle Reducer received FDA 510(k) clearance on 2022-04-02, under 510(k) number K212947.
Who is the listed applicant for Trinity Plus Wrinkle Reducer?
The FDA 510(k) record lists Carol Cole Company Dba Nuface as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trinity Plus Wrinkle Reducer?
The FDA product code for Trinity Plus Wrinkle Reducer is OHS.
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Carol Cole Company Dba Nuface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：OHS）
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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官方来源
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