植入性自主神經刺激器，用於中風復健
PMA 核准號：P210007 · 2026-09-16
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器材摘要
Stimulator, autonomic nerve, implanted for stroke rehabilitation is the device name listed in this FDA 510(k) record. The listed applicant is Mobia Medical, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code QPY. It was reviewed by the PM advisory panel.
常見問題
What is the Stimulator, autonomic nerve, implanted for stroke rehabilitation?
Stimulator, autonomic nerve, implanted for stroke rehabilitation is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Mobia Medical, Inc..
When did Stimulator, autonomic nerve, implanted for stroke rehabilitation receive FDA 510(k) clearance?
The clearance date for Stimulator, autonomic nerve, implanted for stroke rehabilitation can be found in the official FDA records.
誰是Stimulator, 自主神經, 經植入治療中風復健的登記申請人？
The FDA 510(k) record lists Mobia Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為什麼是為了中風復健植入的自主神經刺激器？
FDA產品代碼為用於中風復健的自律神經刺激器的產品代碼為QPY。
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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