可植入式心臟除颤器（非CRT）
PMA 核准號：P960040 · 2026-08-25
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器材摘要
Implantable cardioverter defibrillator (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 2026-08-25. The device is classified under product code LWS. It was reviewed by the CV advisory panel.
常見問題
What is the Implantable cardioverter defibrillator (non-CRT)?
Implantable cardioverter defibrillator (non-CRT) is a medical device that received FDA 510(k) clearance on 2026-08-25. The listed applicant is Boston Scientific.
When did Implantable cardioverter defibrillator (non-CRT) receive FDA 510(k) clearance?
The clearance date for Implantable cardioverter defibrillator (non-CRT) can be found in the official FDA records.
誰是可植入式心臟除颤器（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。
植入式心臟去極化器（非CRT）的FDA產品代碼是什麼？
FDA產品代碼對於植入式心臟去節律器（非CRT）為LWS。
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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