刺激器，舌下神經，植入式，呼吸中止
PMA 核准號：P240024 · 2026-07-30
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器材摘要
Stimulator, hypoglossal nerve, implanted, apnea is the device name listed in this FDA 510(k) record. The listed applicant is Nyxoah S.A.. It received FDA 510(k) clearance on 2026-07-30. The device is classified under product code MNQ. It was reviewed by the AN advisory panel.
常見問題
What is the Stimulator, hypoglossal nerve, implanted, apnea?
Stimulator, hypoglossal nerve, implanted, apnea is a medical device that received FDA 510(k) clearance on 2026-07-30. The listed applicant is Nyxoah S.A..
When did Stimulator, hypoglossal nerve, implanted, apnea receive FDA 510(k) clearance?
The clearance date for Stimulator, hypoglossal nerve, implanted, apnea can be found in the official FDA records.
誰是植入性舌下神經刺激器，呼吸中止的列名申請人？
The FDA 510(k) record lists Nyxoah S.A. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為什麼是Stimulator, hypoglossal nerve, implanted, apnea？
FDA產品代碼為Stimulator, hypoglossal nerve, implanted, apnea的MNQ。
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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