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FDA 510(k)

CentriMag 循環輔助系統，CentriMag 返流（動脈）針管套件，CentriMag 排液（靜脈）針管套件

K 號：K200306 · 2020-03-06

申請人Abbott (Formerly Thoratec Corporation)
決定日期2020-03-06
產品代碼DWA
諮詢委員會履歷
決定相當於

器材摘要

CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit is the device name listed in this FDA 510(k) record. The listed applicant is Abbott (Formerly Thoratec Corporation). It received FDA 510(k) clearance on 2020-03-06 under 510(k) number K200306. The device is classified under product code DWA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit?

CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit is a medical device that received FDA 510(k) clearance on 2020-03-06. The listed applicant is Abbott (Formerly Thoratec Corporation). The 510(k) number is K200306.

When did CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit receive FDA 510(k) clearance?

CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit received FDA 510(k) clearance on 2020-03-06, under 510(k) number K200306.

Who is the listed applicant for CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit?

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

What is the FDA product code for CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit?

The FDA product code for CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit is DWA.

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

其他以 Abbott (Formerly Thoratec Corporation) 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。

K222038CentriMag™ 血液泵，適用於與CentriMag™ 急性循環支持系統使用

相關器械（代碼：DWA）

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。

K232788INSPiRA ART100Inspira Technologies Oxy B.H.N. , Ltd.K230698Anivia SG1000 泵控制台Apmtd, Inc.K221491Anivia SG1000 泵控制台Apmtd, Inc.K192838量子離心驅動-高壓，量子離心驅動-中壓Spectrum Medical , Ltd.K191557CentriMag 急性循環支持系統Thoratec Corporation (Now Part of Abbott)

官方來源

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