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FDA 510(k)

CAPERE 靈栓切除系統

K 號：K180722 · 2018-06-11

申請人Kp Medcure, Inc.
決定日期2018-06-11
產品代碼QEW
諮詢委員會履歷
決定相當於

器材摘要

CAPERE Thrombectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Kp Medcure, Inc.. It received FDA 510(k) clearance on 2018-06-11 under 510(k) number K180722. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CAPERE Thrombectomy System?

CAPERE Thrombectomy System is a medical device that received FDA 510(k) clearance on 2018-06-11. The listed applicant is Kp Medcure, Inc.. The 510(k) number is K180722.

When did CAPERE Thrombectomy System receive FDA 510(k) clearance?

CAPERE Thrombectomy System received FDA 510(k) clearance on 2018-06-11, under 510(k) number K180722.

Who is the listed applicant for CAPERE Thrombectomy System?

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

What is the FDA product code for CAPERE Thrombectomy System?

The FDA product code for CAPERE Thrombectomy System is QEW.

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：QEW）

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。

K253419Triever Duo 穿刺針管Inari Medical, Inc.K261800Helo Max 靈栓切除系統 (HEL2090)Endovascular EngineeringK262538Artix™ MT;Artix™ Thin-Walled SheathInari Medical, Inc.K261523Vertex™ 靈栓切除系統Jupiter EndovascularK260599INDIGO® 吸引系統 – INDIGO 鏈接Penumbra, Inc.K251949INDIGO® 吸引系統 - 雷電閃吸管連結版Penumbra, Inc.

官方來源

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