視窗作業系統，視窗AI掃描，RTHawk
K 號：K251029 · 2025-08-21
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器材摘要
Vista OS, Vista AI Scan, RTHawk is the device name listed in this FDA 510(k) record. The listed applicant is Vista AI, Inc.. It received FDA 510(k) clearance on 2025-08-21 under 510(k) number K251029. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Vista OS, Vista AI Scan, RTHawk?
Vista OS, Vista AI Scan, RTHawk is a medical device that received FDA 510(k) clearance on 2025-08-21. The listed applicant is Vista AI, Inc.. The 510(k) number is K251029.
When did Vista OS, Vista AI Scan, RTHawk receive FDA 510(k) clearance?
Vista OS, Vista AI Scan, RTHawk received FDA 510(k) clearance on 2025-08-21, under 510(k) number K251029.
Who is the listed applicant for Vista OS, Vista AI Scan, RTHawk?
The FDA 510(k) record lists Vista AI, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vista OS, Vista AI Scan, RTHawk?
The FDA product code for Vista OS, Vista AI Scan, RTHawk is LNH.
相關臨床試驗
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相關器械（代碼：LNH）
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。
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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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