BeneLife 預紀元面部護理組合，型號：QZ0701A
K 號：K171647 · 2017-10-23
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器材摘要
常見問題
What is the BeneLife Premium Facial Treatment Pack, Model: QZ0701A?
BeneLife Premium Facial Treatment Pack, Model: QZ0701A is a medical device that received FDA 510(k) clearance on 2017-10-23. The listed applicant is Infinitus (China) Company , Ltd.. The 510(k) number is K171647.
When did BeneLife Premium Facial Treatment Pack, Model: QZ0701A receive FDA 510(k) clearance?
BeneLife Premium Facial Treatment Pack, Model: QZ0701A received FDA 510(k) clearance on 2017-10-23, under 510(k) number K171647.
Who is the listed applicant for BeneLife Premium Facial Treatment Pack, Model: QZ0701A?
The FDA 510(k) record lists Infinitus (China) Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BeneLife Premium Facial Treatment Pack, Model: QZ0701A?
The FDA product code for BeneLife Premium Facial Treatment Pack, Model: QZ0701A is NFO.
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：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。
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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