CT Expres 3D 郵遞媒質系統,瓶針型 B,日設 III HP,病人設備
K 號:K151048 · 2016-01-22
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器材摘要
常見問題
What is the CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set?
CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set is a medical device that received FDA 510(k) clearance on 2016-01-22. The listed applicant is Bracco Injeneering. The 510(k) number is K151048.
When did CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set receive FDA 510(k) clearance?
CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set received FDA 510(k) clearance on 2016-01-22, under 510(k) number K151048.
Who is the listed applicant for CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set?
The FDA 510(k) record lists Bracco Injeneering as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set?
The FDA product code for CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set is IZQ.
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相關器械(代碼:IZQ)
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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