超扭力MB血管造影導管,配以顯影標記帶
K 號:K212977 · 2022-02-17
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器材摘要
常見問題
What is the SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands?
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands is a medical device that received FDA 510(k) clearance on 2022-02-17. The listed applicant is Cordis Corporation. The 510(k) number is K212977.
When did SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands receive FDA 510(k) clearance?
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands received FDA 510(k) clearance on 2022-02-17, under 510(k) number K212977.
Who is the listed applicant for SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands?
The FDA 510(k) record lists Cordis Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands?
The FDA product code for SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands is DQO.
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 Cordis 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:DQO)
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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