FDA 510(k)

心臟觸發監測器，心臟與規範同步監測器

K 號：K151781 · 2016-05-27

決定日期2016-05-27

產品代碼DRT

諮詢委員會履歷

決定相當於

器材摘要

Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Ivy Biomedical Systems, Inc.. It received FDA 510(k) clearance on 2016-05-27 under 510(k) number K151781. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor?

Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor is a medical device that received FDA 510(k) clearance on 2016-05-27. The listed applicant is Ivy Biomedical Systems, Inc.. The 510(k) number is K151781.

When did Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor receive FDA 510(k) clearance?

Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor received FDA 510(k) clearance on 2016-05-27, under 510(k) number K151781.

Who is the listed applicant for Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor?

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

What is the FDA product code for Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor?

The FDA product code for Cardiac Trigger Monitor, Cardiac & Regulatory Synchronization Monitor is DRT.

其他以 Ivy Biomedical Systems, 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。

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相關器械（代碼：DRT）

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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