NuFACE Mini Plus
K 號：K201680 · 2021-02-19
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器材摘要
NuFACE Mini Plus is the device name listed in this FDA 510(k) record. The listed applicant is Carole Cole Company. It received FDA 510(k) clearance on 2021-02-19 under 510(k) number K201680. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NuFACE Mini Plus?
NuFACE Mini Plus is a medical device that received FDA 510(k) clearance on 2021-02-19. The listed applicant is Carole Cole Company. The 510(k) number is K201680.
When did NuFACE Mini Plus receive FDA 510(k) clearance?
NuFACE Mini Plus received FDA 510(k) clearance on 2021-02-19, under 510(k) number K201680.
Who is the listed applicant for NuFACE Mini Plus?
The FDA 510(k) record lists Carole Cole Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NuFACE Mini Plus?
The FDA product code for NuFACE Mini Plus is NFO.
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相關器械（代碼：NFO）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
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