InterView XP；InterView FUSION
K 號：K221984 · 2023-03-29
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器材摘要
InterView XP; InterView FUSION is the device name listed in this FDA 510(k) record. The listed applicant is Mediso Medical Imaging Systems, Lttd.. It received FDA 510(k) clearance on 2023-03-29 under 510(k) number K221984. 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 InterView XP; InterView FUSION?
InterView XP; InterView FUSION is a medical device that received FDA 510(k) clearance on 2023-03-29. The listed applicant is Mediso Medical Imaging Systems, Lttd.. The 510(k) number is K221984.
When did InterView XP; InterView FUSION receive FDA 510(k) clearance?
InterView XP; InterView FUSION received FDA 510(k) clearance on 2023-03-29, under 510(k) number K221984.
Who is the listed applicant for InterView XP; InterView FUSION?
The FDA 510(k) record lists Mediso Medical Imaging Systems, Lttd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InterView XP; InterView FUSION?
The FDA product code for InterView XP; InterView FUSION is LLZ.
相關臨床試驗
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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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