vRad 查覽器
K 號：K241879 · 2024-07-18
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器材摘要
vRad Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Radiologic Corporation. It received FDA 510(k) clearance on 2024-07-18 under 510(k) number K241879. 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 vRad Viewer?
vRad Viewer is a medical device that received FDA 510(k) clearance on 2024-07-18. The listed applicant is Virtual Radiologic Corporation. The 510(k) number is K241879.
When did vRad Viewer receive FDA 510(k) clearance?
vRad Viewer received FDA 510(k) clearance on 2024-07-18, under 510(k) number K241879.
Who is the listed applicant for vRad Viewer?
The FDA 510(k) record lists Virtual Radiologic Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for vRad Viewer?
The FDA product code for vRad Viewer is LLZ.
相關臨床試驗
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其他以 Virtual Radiologic Corporation 為申請人之記錄
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。
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