FDA 510(k)

uAI Portal

K 號：K240411 · 2024-09-06

申請人Shanghai United Imaging Intelligence Co., Ltd.

決定日期2024-09-06

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

uAI Portal is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai United Imaging Intelligence Co., Ltd.. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K240411. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the uAI Portal?

uAI Portal is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Shanghai United Imaging Intelligence Co., Ltd.. The 510(k) number is K240411.

When did uAI Portal receive FDA 510(k) clearance?

uAI Portal received FDA 510(k) clearance on 2024-09-06, under 510(k) number K240411.

Who is the listed applicant for uAI Portal?

The FDA 510(k) record lists Shanghai United Imaging Intelligence Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for uAI Portal?

The FDA product code for uAI Portal is QIH.

其他以 Shanghai United Imaging Intelligence Co., Ltd. 為申請人之記錄

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。

K242292uAI 輕鬆分類 ICH K222755uMR 680 K193271uAI EasyTriage-Rib

相關器械（代碼：QIH）

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。

K260055syngo.CT 脑量化Siemens Medical Solutions USA, Inc.K262390骨專家Visiana K261368快速平台（R6.7）Ischemaview, Inc.K261623EchoPAC 軟體僅 / EchoPAC 插件（v211）GE Medical Systems Ultrasound and Primary Care Diagnostics K261677人工智慧腎臟評估（AIRA）版本 1Aramis Global AI Consultancies, LLC K2608794DMINVIA, LLC

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。