FDA 510(k)

ARIETTA 50

K 號：K220295 · 2022-04-29

決定日期2022-04-29

產品代碼IYN

諮詢委員會RA

決定相當於

器材摘要

ARIETTA 50 is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Healthcare Corporation. It received FDA 510(k) clearance on 2022-04-29 under 510(k) number K220295. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ARIETTA 50?

ARIETTA 50 is a medical device that received FDA 510(k) clearance on 2022-04-29. The listed applicant is Fujifilm Healthcare Corporation. The 510(k) number is K220295.

When did ARIETTA 50 receive FDA 510(k) clearance?

ARIETTA 50 received FDA 510(k) clearance on 2022-04-29, under 510(k) number K220295.

Who is the listed applicant for ARIETTA 50?

The FDA 510(k) record lists Fujifilm Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARIETTA 50?

The FDA product code for ARIETTA 50 is IYN.

其他以 Fujifilm Healthcare Corporation 為申請人之記錄

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相關器械（代碼：IYN）

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

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