刺激器，自律神經，植入用於癲癇
PMA 核准號：P970003 · 2026-08-12
廣告
決定日期2026-08-12
PMA 編號P970003
產品代碼LYJ
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, autonomic nerve, implanted for epilepsy is the device name listed in this FDA 510(k) record. The listed applicant is LivaNova USA, Inc.. It received FDA 510(k) clearance on 2026-08-12. The device is classified under product code LYJ. It was reviewed by the NE advisory panel.
常見問題
What is the Stimulator, autonomic nerve, implanted for epilepsy?
Stimulator, autonomic nerve, implanted for epilepsy is a medical device that received FDA 510(k) clearance on 2026-08-12. The listed applicant is LivaNova USA, Inc..
When did Stimulator, autonomic nerve, implanted for epilepsy receive FDA 510(k) clearance?
The clearance date for Stimulator, autonomic nerve, implanted for epilepsy can be found in the official FDA records.
Who is the listed applicant for Stimulator, autonomic nerve, implanted for epilepsy?
The FDA 510(k) record lists LivaNova USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, autonomic nerve, implanted for epilepsy?
The FDA product code for Stimulator, autonomic nerve, implanted for epilepsy is LYJ.
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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