Ventricular (assist) bypass
PMA 核准號：P100047 · 2026-09-23
廣告
器材摘要
Ventricular (assist) bypass is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic. It received FDA 510(k) clearance on 2026-09-23. The device is classified under product code DSQ. It was reviewed by the CV advisory panel.
常見問題
What is the Ventricular (assist) bypass?
Ventricular (assist) bypass is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is Medtronic.
When did Ventricular (assist) bypass receive FDA 510(k) clearance?
The clearance date for Ventricular (assist) bypass can be found in the official FDA records.
Who is the listed applicant for Ventricular (assist) bypass?
The FDA 510(k) record lists Medtronic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ventricular (assist) bypass?
The FDA product code for Ventricular (assist) bypass is DSQ.
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 Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751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
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
廣告