NuFACE膠質底霜
K 號：K161654 · 2016-12-30
廣告
器材摘要
NuFACE Gel Primer is the device name listed in this FDA 510(k) record. The listed applicant is Carol Cole Company. It received FDA 510(k) clearance on 2016-12-30 under 510(k) number K161654. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NuFACE Gel Primer?
NuFACE Gel Primer is a medical device that received FDA 510(k) clearance on 2016-12-30. The listed applicant is Carol Cole Company. The 510(k) number is K161654.
When did NuFACE Gel Primer receive FDA 510(k) clearance?
NuFACE Gel Primer received FDA 510(k) clearance on 2016-12-30, under 510(k) number K161654.
Who is the listed applicant for NuFACE Gel Primer?
The FDA 510(k) record lists Carol Cole Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NuFACE Gel Primer?
The FDA product code for NuFACE Gel Primer is GYB.
相關臨床試驗
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：GYB）
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。
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。
廣告