ibiomedi 電子聽診器 ES-2020
K 號：K220466 · 2022-11-03
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器材摘要
ibiomedi Electronic Stethoscope ES-2020 is the device name listed in this FDA 510(k) record. The listed applicant is Sound Land Corp.. It received FDA 510(k) clearance on 2022-11-03 under 510(k) number K220466. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ibiomedi Electronic Stethoscope ES-2020?
ibiomedi Electronic Stethoscope ES-2020 is a medical device that received FDA 510(k) clearance on 2022-11-03. The listed applicant is Sound Land Corp.. The 510(k) number is K220466.
When did ibiomedi Electronic Stethoscope ES-2020 receive FDA 510(k) clearance?
ibiomedi Electronic Stethoscope ES-2020 received FDA 510(k) clearance on 2022-11-03, under 510(k) number K220466.
Who is the listed applicant for ibiomedi Electronic Stethoscope ES-2020?
The FDA 510(k) record lists Sound Land Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ibiomedi Electronic Stethoscope ES-2020?
The FDA product code for ibiomedi Electronic Stethoscope ES-2020 is DQD.
相關臨床試驗
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相關器械（代碼：DQD）
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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