ArgenZ 液體顏色調節劑, ArgenZ 齿尖效果, ArgenZ 颜色調節劑, ArgenZ 桥梁減色劑
K 號:K182833 · 2019-02-08
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器材摘要
常見問題
What is the ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer?
ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer is a medical device that received FDA 510(k) clearance on 2019-02-08. The listed applicant is The Argen Corporation. The 510(k) number is K182833.
When did ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer receive FDA 510(k) clearance?
ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer received FDA 510(k) clearance on 2019-02-08, under 510(k) number K182833.
Who is the listed applicant for ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer?
The FDA 510(k) record lists The Argen Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer?
The FDA product code for ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer is EIH.
相關臨床試驗
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其他以 The Argen Corporation 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:EIH)
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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