多靈通耳鳴技術
K 號：K201370 · 2020-06-19
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決定日期2020-06-19
產品代碼KLW
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
Multiflex Tinnitus Technology is the device name listed in this FDA 510(k) record. The listed applicant is Starkey Laboratories, Inc.. It received FDA 510(k) clearance on 2020-06-19 under 510(k) number K201370. The device is classified under product code KLW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Multiflex Tinnitus Technology?
Multiflex Tinnitus Technology is a medical device that received FDA 510(k) clearance on 2020-06-19. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K201370.
When did Multiflex Tinnitus Technology receive FDA 510(k) clearance?
Multiflex Tinnitus Technology received FDA 510(k) clearance on 2020-06-19, under 510(k) number K201370.
Who is the listed applicant for Multiflex Tinnitus Technology?
The FDA 510(k) record lists Starkey Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Multiflex Tinnitus Technology?
The FDA product code for Multiflex Tinnitus Technology is KLW.
相關臨床試驗
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相關器械（代碼：KLW）
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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