FDA 510(k)

AI4CMR v1.0

K 號：K220624 · 2022-07-22

決定日期2022-07-22

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

AI4CMR v1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Ai4medimaging Medical Solutions S.A.. It received FDA 510(k) clearance on 2022-07-22 under 510(k) number K220624. 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 AI4CMR v1.0?

AI4CMR v1.0 is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Ai4medimaging Medical Solutions S.A.. The 510(k) number is K220624.

When did AI4CMR v1.0 receive FDA 510(k) clearance?

AI4CMR v1.0 received FDA 510(k) clearance on 2022-07-22, under 510(k) number K220624.

Who is the listed applicant for AI4CMR v1.0?

The FDA 510(k) record lists Ai4medimaging Medical Solutions S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AI4CMR v1.0?

The FDA product code for AI4CMR v1.0 is LLZ.

其他以 Ai4medimaging Medical Solutions S.A. 為申請人之記錄

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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。

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官方來源

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