快速射線
K 號：K242838 · 2025-02-21
廣告
器材摘要
QuickRad is the device name listed in this FDA 510(k) record. The listed applicant is Aikenist Technologies Pvt, Ltd.. It received FDA 510(k) clearance on 2025-02-21 under 510(k) number K242838. 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 QuickRad?
QuickRad is a medical device that received FDA 510(k) clearance on 2025-02-21. The listed applicant is Aikenist Technologies Pvt, Ltd.. The 510(k) number is K242838.
When did QuickRad receive FDA 510(k) clearance?
QuickRad received FDA 510(k) clearance on 2025-02-21, under 510(k) number K242838.
Who is the listed applicant for QuickRad?
The FDA 510(k) record lists Aikenist Technologies Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QuickRad?
The FDA product code for QuickRad 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