強脉冲光（IPL）系統，型號：T023K、T023A、T023B、T023C、T023D、T023E、T021K、T021A、T001A、T001B、T001M、T001N、T011C、T016K
K 號：K223928 · 2023-03-28
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器材摘要
常見問題
What is the Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K?
Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K is a medical device that received FDA 510(k) clearance on 2023-03-28. The listed applicant is Shenzhen Fansizhe Science and Technology Co., Ltd.. The 510(k) number is K223928.
When did Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K receive FDA 510(k) clearance?
Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K received FDA 510(k) clearance on 2023-03-28, under 510(k) number K223928.
Who is the listed applicant for Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K?
The FDA 510(k) record lists Shenzhen Fansizhe Science and Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K?
The FDA product code for Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K is OHT.
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其他以 Shenzhen Fansizhe Science and Technology Co., Ltd. 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：OHT）
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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