FDA 510(k)

µCor 心衰竭與心律不整管理系統

K 號：K172510 · 2018-05-11

決定日期2018-05-11

產品代碼MHX

諮詢委員會履歷

決定相當於

器材摘要

µCor Heart Failure and Arrhythmia Management System is the device name listed in this FDA 510(k) record. The listed applicant is Zoll Manufacturing Corporation. It received FDA 510(k) clearance on 2018-05-11 under 510(k) number K172510. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the µCor Heart Failure and Arrhythmia Management System?

µCor Heart Failure and Arrhythmia Management System is a medical device that received FDA 510(k) clearance on 2018-05-11. The listed applicant is Zoll Manufacturing Corporation. The 510(k) number is K172510.

When did µCor Heart Failure and Arrhythmia Management System receive FDA 510(k) clearance?

µCor Heart Failure and Arrhythmia Management System received FDA 510(k) clearance on 2018-05-11, under 510(k) number K172510.

Who is the listed applicant for µCor Heart Failure and Arrhythmia Management System?

The FDA 510(k) record lists Zoll Manufacturing Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for µCor Heart Failure and Arrhythmia Management System?

The FDA product code for µCor Heart Failure and Arrhythmia Management System is MHX.

其他以 Zoll Manufacturing Corporation 為申請人之記錄

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K190939ZOLL心律管理系統 K182093ZOLL 心電圖分析軟體

相關器械（代碼：MHX）

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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