感測器，葡萄糖，侵入式
PMA 核准號：P120005 · 2024-01-09
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器材摘要
Sensor, glucose, invasive is the device name listed in this FDA 510(k) record. The listed applicant is Dexcom, Inc.. It received FDA 510(k) clearance on 2024-01-09. The device is classified under product code MDS. It was reviewed by the CH advisory panel.
常見問題
What is the Sensor, glucose, invasive?
Sensor, glucose, invasive is a medical device that received FDA 510(k) clearance on 2024-01-09. The listed applicant is Dexcom, Inc..
When did Sensor, glucose, invasive receive FDA 510(k) clearance?
The clearance date for Sensor, glucose, invasive can be found in the official FDA records.
誰是Sensor,葡萄糖，侵入式所列申請人？
FDA 510(k) 記錄將 Dexcom, Inc. 列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為Sensor,葡萄糖，侵入式是什麼？
FDA產品代碼為Sensor,葡萄糖，侵入式為MDS。
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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