QuickScreen Pro 多藥檢測試劑,型號 9395Z
K 號:K181945 · 2018-10-18
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器材摘要
常見問題
What is the QuickScreen Pro Multi Drug Screening Test, Model 9395Z?
QuickScreen Pro Multi Drug Screening Test, Model 9395Z is a medical device that received FDA 510(k) clearance on 2018-10-18. The listed applicant is Phamatech, Inc.. The 510(k) number is K181945.
When did QuickScreen Pro Multi Drug Screening Test, Model 9395Z receive FDA 510(k) clearance?
QuickScreen Pro Multi Drug Screening Test, Model 9395Z received FDA 510(k) clearance on 2018-10-18, under 510(k) number K181945.
Who is the listed applicant for QuickScreen Pro Multi Drug Screening Test, Model 9395Z?
The FDA 510(k) record lists Phamatech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QuickScreen Pro Multi Drug Screening Test, Model 9395Z?
The FDA product code for QuickScreen Pro Multi Drug Screening Test, Model 9395Z is DKZ.
相關臨床試驗
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相關器械(代碼:DKZ)
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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