可植入式脈搏發生器，起搏器（非CRT）
PMA 核准號：P840068 · 2021-04-02
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器材摘要
Implantable pulse generator, pacemaker (non-CRT) is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific. It received FDA 510(k) clearance on 2021-04-02. The device is classified under product code LWP. It was reviewed by the CV advisory panel.
常見問題
What is the Implantable pulse generator, pacemaker (non-CRT)?
Implantable pulse generator, pacemaker (non-CRT) is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is Boston Scientific.
When did Implantable pulse generator, pacemaker (non-CRT) receive FDA 510(k) clearance?
The clearance date for Implantable pulse generator, pacemaker (non-CRT) can be found in the official FDA records.
誰是植入式脈衝發生器、起搏器（非CRT）的登記申請人？
FDA 510(k) 記錄將波士頓科學公司列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為植入式脈搏發生器，起搏器（非CRT）是什麼？
FDA產品代碼對於植入式脈搏發生器、起搏器（非CRT）為LWP。
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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