消融針，腎神經阻斷
PMA 核准號：P220026 · 2026-09-10
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器材摘要
Ablation catheter, renal denervation is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2026-09-10. The device is classified under product code QYI. It was reviewed by the CV advisory panel.
常見問題
What is the Ablation catheter, renal denervation?
Ablation catheter, renal denervation is a medical device that received FDA 510(k) clearance on 2026-09-10. The listed applicant is Medtronic, Inc..
When did Ablation catheter, renal denervation receive FDA 510(k) clearance?
The clearance date for Ablation catheter, renal denervation can be found in the official FDA records.
誰是消融針、腎神經調節的登記申請人？
FDA 510(k) 記錄將美敦力公司（Medtronic, Inc.）列為申請人。這並不單獨確立該設備製造商。
FDA產品代碼為Ablation catheter, 腎神經消融器的產品代碼是什麼？
FDA產品代碼為Ablation catheter, renal denervation的產品為QYI。
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。
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。
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