免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA PMA

內置性癲癇腦刺激器

PMA 核准號:P100026 · 2026-08-19

決定日期2026-08-19
PMA 編號P100026
產品代碼PFN
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

Implanted brain stimulator for epilepsy is the device name listed in this FDA 510(k) record. The listed applicant is NeuroPace, Inc.. It received FDA 510(k) clearance on 2026-08-19. The device is classified under product code PFN. It was reviewed by the NE advisory panel.

常見問題

What is the Implanted brain stimulator for epilepsy?

Implanted brain stimulator for epilepsy is a medical device that received FDA 510(k) clearance on 2026-08-19. The listed applicant is NeuroPace, Inc..

When did Implanted brain stimulator for epilepsy receive FDA 510(k) clearance?

The clearance date for Implanted brain stimulator for epilepsy can be found in the official FDA records.

Who is the listed applicant for Implanted brain stimulator for epilepsy?

The FDA 510(k) record lists NeuroPace, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implanted brain stimulator for epilepsy?

The FDA product code for Implanted brain stimulator for epilepsy is PFN.

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。

↑