FDA 510(k)

維特瑞亞CT VScore

K 號：K243240 · 2025-04-10

決定日期2025-04-10

產品代碼JAK

諮詢委員會RA

決定相當於

器材摘要

Vitrea CT VScore is the device name listed in this FDA 510(k) record. The listed applicant is Canon Medical Informatics, Inc.. It received FDA 510(k) clearance on 2025-04-10 under 510(k) number K243240. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vitrea CT VScore?

Vitrea CT VScore is a medical device that received FDA 510(k) clearance on 2025-04-10. The listed applicant is Canon Medical Informatics, Inc.. The 510(k) number is K243240.

When did Vitrea CT VScore receive FDA 510(k) clearance?

Vitrea CT VScore received FDA 510(k) clearance on 2025-04-10, under 510(k) number K243240.

Who is the listed applicant for Vitrea CT VScore?

The FDA 510(k) record lists Canon Medical Informatics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vitrea CT VScore?

The FDA product code for Vitrea CT VScore is JAK.

其他以 Canon Medical Informatics, Inc. 為申請人之記錄

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K260324Vitrea CT 穿刺性主動脈瓣置換術 (TAVR) 规劃 K252217CT VScore+K223261開放式肋骨 K222662維特瑞亞CT心臟分析

相關器械（代碼：JAK）

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。

K261125BodyTom 64 (NL4100)；OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA 觀察階段 6.0Fujifilm Corporation K253836FCT iStream 階段 2Fujifilm Corporation K253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung Company K253770卡迪克套件GE Medical Systems SCS K253560強化版PCCT邊界Ge Medical Systems, LLC

官方來源

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