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FDA 510(k)

ROSC-U Mini 胸部壓縮器（RMCC）

K 號：K153628 · 2016-01-30

申請人Resuscitation International, LLC
決定日期2016-01-30
產品代碼DRM
諮詢委員會履歷
決定相當於

器材摘要

ROSC-U Mini Chest Compressor (RMCC) is the device name listed in this FDA 510(k) record. The listed applicant is Resuscitation International, LLC. It received FDA 510(k) clearance on 2016-01-30 under 510(k) number K153628. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ROSC-U Mini Chest Compressor (RMCC)?

ROSC-U Mini Chest Compressor (RMCC) is a medical device that received FDA 510(k) clearance on 2016-01-30. The listed applicant is Resuscitation International, LLC. The 510(k) number is K153628.

When did ROSC-U Mini Chest Compressor (RMCC) receive FDA 510(k) clearance?

ROSC-U Mini Chest Compressor (RMCC) received FDA 510(k) clearance on 2016-01-30, under 510(k) number K153628.

Who is the listed applicant for ROSC-U Mini Chest Compressor (RMCC)?

The FDA 510(k) record lists Resuscitation International, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROSC-U Mini Chest Compressor (RMCC)?

The FDA product code for ROSC-U Mini Chest Compressor (RMCC) is DRM.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

相關器械（代碼：DRM）

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。

K221700AutoPulse NXT 救援系統Zoll Circulation, Inc.K211289RMU-2000自動胸部壓縮系統Defibtech, LLCK173553LUCAS 3 胸部壓縮系統Jolife ABK161768LUCAS 3 胸部壓縮系統Jolife AB

官方來源

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