Examion X-AQS
K 號：K170729 · 2017-07-18
廣告
器材摘要
Examion X-AQS is the device name listed in this FDA 510(k) record. The listed applicant is Examion GmbH. It received FDA 510(k) clearance on 2017-07-18 under 510(k) number K170729. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Examion X-AQS?
Examion X-AQS is a medical device that received FDA 510(k) clearance on 2017-07-18. The listed applicant is Examion GmbH. The 510(k) number is K170729.
When did Examion X-AQS receive FDA 510(k) clearance?
Examion X-AQS received FDA 510(k) clearance on 2017-07-18, under 510(k) number K170729.
Who is the listed applicant for Examion X-AQS?
The FDA 510(k) record lists Examion GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Examion X-AQS?
The FDA product code for Examion X-AQS is LLZ.
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：LLZ）
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