MegaVac機械性血栓切除系統
K 號：K171493 · 2017-08-10
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器材摘要
MegaVac Mechanical Thrombectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Capture Vascular, Inc.. It received FDA 510(k) clearance on 2017-08-10 under 510(k) number K171493. The device is classified under product code QEX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MegaVac Mechanical Thrombectomy System?
MegaVac Mechanical Thrombectomy System is a medical device that received FDA 510(k) clearance on 2017-08-10. The listed applicant is Capture Vascular, Inc.. The 510(k) number is K171493.
When did MegaVac Mechanical Thrombectomy System receive FDA 510(k) clearance?
MegaVac Mechanical Thrombectomy System received FDA 510(k) clearance on 2017-08-10, under 510(k) number K171493.
Who is the listed applicant for MegaVac Mechanical Thrombectomy System?
The FDA 510(k) record lists Capture Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MegaVac Mechanical Thrombectomy System?
The FDA product code for MegaVac Mechanical Thrombectomy System is QEX.
相關臨床試驗
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相關器械（代碼：QEX）
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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