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FDA 510(k)

AMC 健康護理系統

K 號:K151839 · 2016-09-09

申請人Amc Health
決定日期2016-09-09
產品代碼MWI
諮詢委員會履歷
決定相當於

器材摘要

AMC Health VitalCaregiving System is the device name listed in this FDA 510(k) record. The listed applicant is Amc Health. It received FDA 510(k) clearance on 2016-09-09 under 510(k) number K151839. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AMC Health VitalCaregiving System?

AMC Health VitalCaregiving System is a medical device that received FDA 510(k) clearance on 2016-09-09. The listed applicant is Amc Health. The 510(k) number is K151839.

When did AMC Health VitalCaregiving System receive FDA 510(k) clearance?

AMC Health VitalCaregiving System received FDA 510(k) clearance on 2016-09-09, under 510(k) number K151839.

Who is the listed applicant for AMC Health VitalCaregiving System?

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

What is the FDA product code for AMC Health VitalCaregiving System?

The FDA product code for AMC Health VitalCaregiving System is MWI.

相關臨床試驗

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其他以 Amc Health 為申請人之記錄

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相關器械(代碼:MWI)

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。

官方來源

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