永久式去颤器電極
PMA 核准號：P920015 · 2026-08-19
廣告
器材摘要
Permanent defibrillator electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2026-08-19. The device is classified under product code NVY. It was reviewed by the CV advisory panel.
常見問題
What is the Permanent defibrillator electrodes?
Permanent defibrillator electrodes is a medical device that received FDA 510(k) clearance on 2026-08-19. The listed applicant is Medtronic, Inc..
When did Permanent defibrillator electrodes receive FDA 510(k) clearance?
The clearance date for Permanent defibrillator electrodes can be found in the official FDA records.
Who is the listed applicant for Permanent defibrillator electrodes?
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。
What is the FDA product code for Permanent defibrillator electrodes?
The FDA product code for Permanent defibrillator electrodes is NVY.
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。
廣告