FLOW-i 麻醉系統 C20，FLOW-i 麻醉系統 C30，FLOW-i 麻醉系統 C40
K 號：K160665 · 2017-03-29
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器材摘要
常見問題
What is the FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40?
FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40 is a medical device that received FDA 510(k) clearance on 2017-03-29. The listed applicant is Maquet Critical Care AB. The 510(k) number is K160665.
When did FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40 receive FDA 510(k) clearance?
FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40 received FDA 510(k) clearance on 2017-03-29, under 510(k) number K160665.
Who is the listed applicant for FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40?
FDA 510(k) 記錄將 Maquet Critical Care AB 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40?
The FDA product code for FLOW-i Anesthesia System C20, FLOW-i Anesthesia System C30, FLOW-i Anesthesia System C40 is BSZ.
相關臨床試驗
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其他以 Maquet Critical Care AB 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：BSZ）
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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