IPL 髮毛去除器,型號:AI01、AI06、AI08、AI16、AI17
K 號:K221466 · 2022-08-12
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器材摘要
常見問題
What is the IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17?
IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17 is a medical device that received FDA 510(k) clearance on 2022-08-12. The listed applicant is Shenzhen Century Dongyuan Technology CO , Ltd.. The 510(k) number is K221466.
When did IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17 receive FDA 510(k) clearance?
IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17 received FDA 510(k) clearance on 2022-08-12, under 510(k) number K221466.
Who is the listed applicant for IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17?
The FDA 510(k) record lists Shenzhen Century Dongyuan Technology CO , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17?
The FDA product code for IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17 is OHT.
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。
其他以 Shenzhen Century Dongyuan 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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