Lifemotion 一次性膠膜氧合器
K 號:K253838 · 2026-03-16
廣告
器材摘要
常見問題
What is the Lifemotion Disposable Membrane Oxygenator?
Lifemotion Disposable Membrane Oxygenator is a medical device that received FDA 510(k) clearance on 2026-03-16. The listed applicant is Lifemotion Medical Technology Co., Ltd.. The 510(k) number is K253838.
When did Lifemotion Disposable Membrane Oxygenator receive FDA 510(k) clearance?
Lifemotion Disposable Membrane Oxygenator received FDA 510(k) clearance on 2026-03-16, under 510(k) number K253838.
Who is the listed applicant for Lifemotion Disposable Membrane Oxygenator?
The FDA 510(k) record lists Lifemotion Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lifemotion Disposable Membrane Oxygenator?
The FDA product code for Lifemotion Disposable Membrane Oxygenator is DTZ.
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。
相關器械(代碼:DTZ)
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。
廣告