syngo.via RT影像套件 VC10
K 號：K252304 · 2026-03-18
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器材摘要
syngo.via RT Image Suite VC10 is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2026-03-18 under 510(k) number K252304. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the syngo.via RT Image Suite VC10?
syngo.via RT Image Suite VC10 is a medical device that received FDA 510(k) clearance on 2026-03-18. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K252304.
When did syngo.via RT Image Suite VC10 receive FDA 510(k) clearance?
syngo.via RT Image Suite VC10 received FDA 510(k) clearance on 2026-03-18, under 510(k) number K252304.
Who is the listed applicant for syngo.via RT Image Suite VC10?
FDA 510(k) 記錄將 Varian Medical Systems, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for syngo.via RT Image Suite VC10?
The FDA product code for syngo.via RT Image Suite VC10 is MUJ.
相關臨床試驗
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其他以 Varian Medical Systems, Inc. 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：MUJ）
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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