感測器，葡萄糖，侵入式，自動胰島素輸送系統之組成部件
PMA 核准號：P250012 · 2026-07-21
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器材摘要
Sensor, Glucose, Invasive, Component of automated insulin delivery system is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed, Inc.. It received FDA 510(k) clearance on 2026-07-21. The device is classified under product code SFI. It was reviewed by the CH advisory panel.
常見問題
What is the Sensor, Glucose, Invasive, Component of automated insulin delivery system?
Sensor, Glucose, Invasive, Component of automated insulin delivery system is a medical device that received FDA 510(k) clearance on 2026-07-21. The listed applicant is Medtronic Minimed, Inc..
When did Sensor, Glucose, Invasive, Component of automated insulin delivery system receive FDA 510(k) clearance?
The clearance date for Sensor, Glucose, Invasive, Component of automated insulin delivery system can be found in the official FDA records.
誰是Sensor, Glucose, Invasive, 自动胰岛素輸送系統組成部件的登記申請人？
The FDA 510(k) record lists Medtronic Minimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為Sensor, Glucose, Invasive, 自动胰岛素输送系统组件的是什麼？
FDA產品代碼為Sensor, Glucose, Invasive, 自动胰岛素输送系统组件的為SFI。
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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