Nu Skin RenuSpa iO
K号: K232001 · 2023-11-21
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决定日期2023-11-21
产品代码NFO
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
Nu Skin RenuSpa iO is the device name listed in this FDA 510(k) record. The listed applicant is Nse Products, Inc.. It received FDA 510(k) clearance on 2023-11-21 under 510(k) number K232001. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nu Skin RenuSpa iO?
Nu Skin RenuSpa iO is a medical device that received FDA 510(k) clearance on 2023-11-21. The listed applicant is Nse Products, Inc.. The 510(k) number is K232001.
When did Nu Skin RenuSpa iO receive FDA 510(k) clearance?
Nu Skin RenuSpa iO received FDA 510(k) clearance on 2023-11-21, under 510(k) number K232001.
Who is the listed applicant for Nu Skin RenuSpa iO?
The FDA 510(k) record lists Nse Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nu Skin RenuSpa iO?
The FDA product code for Nu Skin RenuSpa iO is NFO.
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相关器械（代码：NFO）
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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