電刺激器，植入式，用於帕金森症症狀
PMA 核准號：P150031 · 2026-09-22
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決定日期2026-09-22
PMA 編號P150031
產品代碼NHL
器械分類3 類
醫療專科U
諮詢委員會NE
(請提供完整的英文描述，以便進行翻譯。)
器材摘要
Stimulator, electrical, implanted, for parkinsonian symptoms is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2026-09-22. The device is classified under product code NHL. It was reviewed by the NE advisory panel.
常見問題
What is the Stimulator, electrical, implanted, for parkinsonian symptoms?
Stimulator, electrical, implanted, for parkinsonian symptoms is a medical device that received FDA 510(k) clearance on 2026-09-22. The listed applicant is Boston Scientific Corp.
When did Stimulator, electrical, implanted, for parkinsonian symptoms receive FDA 510(k) clearance?
The clearance date for Stimulator, electrical, implanted, for parkinsonian symptoms can be found in the official FDA records.
誰是Stimulator, electrical, implanted, for parkinsonian symptoms的登記申請人？
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？用於治療帕金森症狀的植入式電刺激器？
FDA產品代碼為電植入式刺激器，用於治療帕金森症狀的產品是NHL。
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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