數位平面面板檢測器
K 號：K230059 · 2023-02-03
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器材摘要
Digital Flat Panel Detector is the device name listed in this FDA 510(k) record. The listed applicant is Ray Imaging Technology (Haining) Limited. It received FDA 510(k) clearance on 2023-02-03 under 510(k) number K230059. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Digital Flat Panel Detector?
Digital Flat Panel Detector is a medical device that received FDA 510(k) clearance on 2023-02-03. The listed applicant is Ray Imaging Technology (Haining) Limited. The 510(k) number is K230059.
When did Digital Flat Panel Detector receive FDA 510(k) clearance?
Digital Flat Panel Detector received FDA 510(k) clearance on 2023-02-03, under 510(k) number K230059.
Who is the listed applicant for Digital Flat Panel Detector?
The FDA 510(k) record lists Ray Imaging Technology (Haining) Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Digital Flat Panel Detector?
The FDA product code for Digital Flat Panel Detector is MQB.
相關臨床試驗
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相關器械（代碼：MQB）
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。
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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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