FDA 510(k)

威爾奇艾倫 Connex® 360 （多個）

K 號：K243598 · 2025-07-13

決定日期2025-07-13

產品代碼

決定相當於

器材摘要

Welch Allyn Connex® 360 (Multiple) is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 2025-07-13 under 510(k) number K243598. FDA Decision: Substantially Equivalent.

常見問題

What is the Welch Allyn Connex® 360 (Multiple)?

Welch Allyn Connex® 360 (Multiple) is a medical device that received FDA 510(k) clearance on 2025-07-13. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K243598.

When did Welch Allyn Connex® 360 (Multiple) receive FDA 510(k) clearance?

Welch Allyn Connex® 360 (Multiple) received FDA 510(k) clearance on 2025-07-13, under 510(k) number K243598.

Who is the listed applicant for Welch Allyn Connex® 360 (Multiple)?

The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.

其他以 Welch Allyn, Inc. 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。

K241411威爾奇艾倫Connex® Spot Monitor；901058生命徵象監測器核心（CSM）K223381iExaminer System with Panoptic Plus K212473威爾奇艾倫 Connex 中心站 K191013威爾奇艾倫診斷心臟學套件 2.X.X 內含肺功能檢查選項 K181016Welch Allyn RetinaVue 網路參考編號 901108 PACS 医學影像系統 K171621威爾奇艾倫 Connex 生化指標監測器，威爾奇艾倫 Connex 集成式牆壁系統，901060 生化指標監測器

查看所有 7 項裝置 →

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。

器材摘要

常見問題

相關臨床試驗

其他以 Welch Allyn, Inc. 為申請人之記錄

官方來源