FDA 510(k)

麥迪森 MX317W-PA

K 號：K242545 · 2025-05-23

決定日期2025-05-23

產品代碼PZZ

諮詢委員會PA

決定相當於

器材摘要

RadiForce MX317W-PA is the device name listed in this FDA 510(k) record. The listed applicant is Eizo Corporation. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K242545. The device is classified under product code PZZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RadiForce MX317W-PA?

RadiForce MX317W-PA is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Eizo Corporation. The 510(k) number is K242545.

When did RadiForce MX317W-PA receive FDA 510(k) clearance?

RadiForce MX317W-PA received FDA 510(k) clearance on 2025-05-23, under 510(k) number K242545.

Who is the listed applicant for RadiForce MX317W-PA?

FDA 510(k) 記錄中將 Eizo Corporation 列為申請人。這並不單獨確立該設備製造商。

What is the FDA product code for RadiForce MX317W-PA?

The FDA product code for RadiForce MX317W-PA is PZZ.

其他以 Eizo Corporation 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。

K262397CuratOR EX2742 K262783麥迪克斯 MX247W K252030RadiForce GX570；RadiForce GX570-AR K243221RadiForce RX570；RadiForce RX570-AR K241441RadiForce RX670；RadiForce RX670-AR K233465麥迪克斯 MX317W

查看所有 23 項裝置 →

相關器械（代碼：PZZ）

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。

K2331198MP 彩色 LCD 屏幕C811W, C811WT, PA27 和 PA27TShenzhen Beacon Display Technology Co., Ltd.K172922MMPC-4127F1Barco N.V.

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。