心臟節律器，永久性，可植入式
PMA 核准號：P890003 · 2026-07-31
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器材摘要
Pulse generator, permanent, implantable is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2026-07-31. The device is classified under product code NVZ. It was reviewed by the CV advisory panel.
常見問題
What is the Pulse generator, permanent, implantable?
Pulse generator, permanent, implantable is a medical device that received FDA 510(k) clearance on 2026-07-31. The listed applicant is Medtronic, Inc..
When did Pulse generator, permanent, implantable receive FDA 510(k) clearance?
The clearance date for Pulse generator, permanent, implantable can be found in the official FDA records.
誰是永久性植入式脈搏發生器的登記申請人？
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 Pulse generator, permanent, implantable 是什麼？
FDA產品代碼，對於永久性植入式脈搏發生器為NVZ。
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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