Lyric4 聽力輔助器
K 號：K232999 · 2024-04-11
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申請人Sonova AG
決定日期2024-04-11
產品代碼ESD
諮詢委員會中文(台灣):
此醫療設備之規範性文件遵循「醫療規範-v1」政策。以下為該文件之翻譯：
此醫療設備已通過美國食品藥品管理局（FDA）的510(k)認證，並獲得PMA許可。該設備的臨床試驗編號為NCTXXXXXXX，並在PubMed上以PMIDXXXXXXX登錄。該設備的識別碼為XXXXXXXX，相關資訊請參考以下網址：[URL]。
公司名稱：[公司名稱]
產品名稱：[產品名稱]
決定相當於
器材摘要
Lyric4 Hearing Aid is the device name listed in this FDA 510(k) record. The listed applicant is Sonova AG. It received FDA 510(k) clearance on 2024-04-11 under 510(k) number K232999. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Lyric4 Hearing Aid?
Lyric4 Hearing Aid is a medical device that received FDA 510(k) clearance on 2024-04-11. The listed applicant is Sonova AG. The 510(k) number is K232999.
When did Lyric4 Hearing Aid receive FDA 510(k) clearance?
Lyric4 Hearing Aid received FDA 510(k) clearance on 2024-04-11, under 510(k) number K232999.
Who is the listed applicant for Lyric4 Hearing Aid?
The FDA 510(k) record lists Sonova AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lyric4 Hearing Aid?
The FDA product code for Lyric4 Hearing Aid is ESD.
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。
其他以 Sonova AG 為申請人之記錄
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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