NuFace 三位一體 Plus 裝置
K 號：K201782 · 2021-01-22
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器材摘要
NuFace Trinity Plus 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 2021-01-22 under 510(k) number K201782. 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 Trinity Plus Device?
NuFace Trinity Plus Device is a medical device that received FDA 510(k) clearance on 2021-01-22. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K201782.
When did NuFace Trinity Plus Device receive FDA 510(k) clearance?
NuFace Trinity Plus Device received FDA 510(k) clearance on 2021-01-22, under 510(k) number K201782.
Who is the listed applicant for NuFace Trinity Plus 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 NuFace Trinity Plus Device?
The FDA product code for NuFace Trinity Plus Device is NFO.
相關臨床試驗
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其他以 Carol Cole Company Dba Nuface 為申請人之記錄
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。
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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