FDA 510(k)

CPRmeter 2 胸外壓急救反饋裝置

K 號：K173886 · 2018-03-23

決定日期2018-03-23

產品代碼LIX

諮詢委員會履歷

決定相當於

器材摘要

CPRmeter 2 CPR Feedback Device is the device name listed in this FDA 510(k) record. The listed applicant is Laerdal Medical AS. It received FDA 510(k) clearance on 2018-03-23 under 510(k) number K173886. The device is classified under product code LIX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CPRmeter 2 CPR Feedback Device?

CPRmeter 2 CPR Feedback Device is a medical device that received FDA 510(k) clearance on 2018-03-23. The listed applicant is Laerdal Medical AS. The 510(k) number is K173886.

When did CPRmeter 2 CPR Feedback Device receive FDA 510(k) clearance?

CPRmeter 2 CPR Feedback Device received FDA 510(k) clearance on 2018-03-23, under 510(k) number K173886.

Who is the listed applicant for CPRmeter 2 CPR Feedback Device?

The FDA 510(k) record lists Laerdal Medical AS as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPRmeter 2 CPR Feedback Device?

The FDA product code for CPRmeter 2 CPR Feedback Device is LIX.

其他以 Laerdal Medical AS 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：LIX）

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。

K201581心肺復甦帶Credo K183348可重用矽膠蓋 CPRmeter 2Laerdal Medical AS

官方來源

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