麻醉氣體機的軟體選項,以達成並維持目標末梢潮氣氧濃度及麻醉劑
PMA 核准號:P210018 · 2022-03-17
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器材摘要
常見問題
What is the Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents?
Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents is a medical device that received FDA 510(k) clearance on 2022-03-17. The listed applicant is Datex-Ohmeda, Inc., A General Electric Company.
When did Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents receive FDA 510(k) clearance?
The clearance date for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents can be found in the official FDA records.
Who is the listed applicant for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents?
The FDA 510(k) record lists Datex-Ohmeda, Inc., A General Electric Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents?
The FDA product code for Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents is QSF.
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。
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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