FDA 510(k)

Argus Cognitive ReVISION 軟體

K 號：K223322 · 2023-07-24

決定日期2023-07-24

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

Argus Cognitive ReVISION Software is the device name listed in this FDA 510(k) record. The listed applicant is Argus Cognitive, Inc.. It received FDA 510(k) clearance on 2023-07-24 under 510(k) number K223322. 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 Argus Cognitive ReVISION Software?

Argus Cognitive ReVISION Software is a medical device that received FDA 510(k) clearance on 2023-07-24. The listed applicant is Argus Cognitive, Inc.. The 510(k) number is K223322.

When did Argus Cognitive ReVISION Software receive FDA 510(k) clearance?

Argus Cognitive ReVISION Software received FDA 510(k) clearance on 2023-07-24, under 510(k) number K223322.

Who is the listed applicant for Argus Cognitive ReVISION Software?

FDA 510(k) 記錄將 Argus Cognitive, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Argus Cognitive ReVISION Software?

The FDA product code for Argus Cognitive ReVISION Software is LLZ.

其他以 Argus Cognitive, Inc. 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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