文東 VC2；文東 VC3
K 號：K223120 · 2024-12-02
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器材摘要
Ventoux VC2; Ventoux VC3 is the device name listed in this FDA 510(k) record. The listed applicant is Flight Medical Innovations , Ltd.. It received FDA 510(k) clearance on 2024-12-02 under 510(k) number K223120. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Ventoux VC2; Ventoux VC3?
Ventoux VC2; Ventoux VC3 is a medical device that received FDA 510(k) clearance on 2024-12-02. The listed applicant is Flight Medical Innovations , Ltd.. The 510(k) number is K223120.
When did Ventoux VC2; Ventoux VC3 receive FDA 510(k) clearance?
Ventoux VC2; Ventoux VC3 received FDA 510(k) clearance on 2024-12-02, under 510(k) number K223120.
Who is the listed applicant for Ventoux VC2; Ventoux VC3?
The FDA 510(k) record lists Flight Medical Innovations , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ventoux VC2; Ventoux VC3?
The FDA product code for Ventoux VC2; Ventoux VC3 is CBK.
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 Flight Medical Innovations , 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：CBK）
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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