FDA 510(k)

Vios監控系統™ 型號 2050；Vios中央站監護器/Vios中央伺服器軟體 2050

K 號：K241728 · 2025-01-23

決定日期2025-01-23

產品代碼DXN

諮詢委員會履歷

決定相當於

器材摘要

Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 is the device name listed in this FDA 510(k) record. The listed applicant is Murata Vios, Inc.. It received FDA 510(k) clearance on 2025-01-23 under 510(k) number K241728. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050?

Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 is a medical device that received FDA 510(k) clearance on 2025-01-23. The listed applicant is Murata Vios, Inc.. The 510(k) number is K241728.

When did Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 receive FDA 510(k) clearance?

Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 received FDA 510(k) clearance on 2025-01-23, under 510(k) number K241728.

Who is the listed applicant for Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050?

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

What is the FDA product code for Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050?

The FDA product code for Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 is DXN.

其他以 Murata Vios, 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。

K232354Vios監控系統™ 型號 2050；Vios中央站監控器/Vios中央伺服器軟體

相關器械（代碼：DXN）

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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