Dochek® 多藥尿液檢測杯;Dochek® 多藥尿液檢測杯 Pro
K 號:K250067 · 2025-02-20
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器材摘要
常見問題
What is the Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro?
Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro is a medical device that received FDA 510(k) clearance on 2025-02-20. The listed applicant is Guangzhou Decheng Biotechnology Co., Ltd.. The 510(k) number is K250067.
When did Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro receive FDA 510(k) clearance?
Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro received FDA 510(k) clearance on 2025-02-20, under 510(k) number K250067.
Who is the listed applicant for Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro?
The FDA 510(k) record lists Guangzhou Decheng Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro?
The FDA product code for Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro is NGL.
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 Guangzhou Decheng Biotechnology 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:NGL)
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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