A5 麻醉系統 (A5);A7 麻醉系統 (A7)
K 號:K253330 · 2026-06-25
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器材摘要
常見問題
What is the A5 Anesthesia System (A5); A7 Anesthesia System (A7)?
A5 Anesthesia System (A5); A7 Anesthesia System (A7) is a medical device that received FDA 510(k) clearance on 2026-06-25. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K253330.
When did A5 Anesthesia System (A5); A7 Anesthesia System (A7) receive FDA 510(k) clearance?
A5 Anesthesia System (A5); A7 Anesthesia System (A7) received FDA 510(k) clearance on 2026-06-25, under 510(k) number K253330.
Who is the listed applicant for A5 Anesthesia System (A5); A7 Anesthesia System (A7)?
The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A5 Anesthesia System (A5); A7 Anesthesia System (A7)?
The FDA product code for A5 Anesthesia System (A5); A7 Anesthesia System (A7) is BSZ.
相關臨床試驗
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其他以 Shenzhen Mindray Bio-Medical Electronics Co., 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: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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