FDA 510(k)

NuBODY 肌肤紧致设备

K号: K171588 · 2017-07-31

决定日期2017-07-31

产品代码NFO

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决定实质等同

器械摘要

NuBODY Skin Toning Device 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 2017-07-31 under 510(k) number K171588. 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 NuBODY Skin Toning Device?

NuBODY Skin Toning Device is a medical device that received FDA 510(k) clearance on 2017-07-31. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K171588.

When did NuBODY Skin Toning Device receive FDA 510(k) clearance?

NuBODY Skin Toning Device received FDA 510(k) clearance on 2017-07-31, under 510(k) number K171588.

Who is the listed applicant for NuBODY Skin Toning Device?

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 NuBODY Skin Toning Device?

The FDA product code for NuBODY Skin Toning Device is NFO.

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。

K240564NuFACE® FIX+K212947Trinity Plus 纹纹减少器 K201906Trinity ELE Plus 及 Trinity ELE Plus Pro K201782NuFace Trinity Plus 设备 K191672NuFACE Mini 设备 K182424NuFACE FIX 皮肤紧致设备

查看所有 8 个设备 →

官方来源

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