雷飛行系統
K 號：K203722 · 2021-09-02
廣告
器材摘要
RayPilot System is the device name listed in this FDA 510(k) record. The listed applicant is Micropos Medical AB. It received FDA 510(k) clearance on 2021-09-02 under 510(k) number K203722. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the RayPilot System?
RayPilot System is a medical device that received FDA 510(k) clearance on 2021-09-02. The listed applicant is Micropos Medical AB. The 510(k) number is K203722.
When did RayPilot System receive FDA 510(k) clearance?
RayPilot System received FDA 510(k) clearance on 2021-09-02, under 510(k) number K203722.
Who is the listed applicant for RayPilot System?
The FDA 510(k) record lists Micropos Medical AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RayPilot System?
The FDA product code for RayPilot System is IYE.
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：IYE）
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