科斯摩斯
K 號：K233826 · 2024-08-29
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器材摘要
Kosmos is the device name listed in this FDA 510(k) record. The listed applicant is EchoNous, Inc.. It received FDA 510(k) clearance on 2024-08-29 under 510(k) number K233826. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Kosmos?
Kosmos is a medical device that received FDA 510(k) clearance on 2024-08-29. The listed applicant is EchoNous, Inc.. The 510(k) number is K233826.
When did Kosmos receive FDA 510(k) clearance?
Kosmos received FDA 510(k) clearance on 2024-08-29, under 510(k) number K233826.
Who is the listed applicant for Kosmos?
The FDA 510(k) record lists EchoNous, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kosmos?
The FDA product code for Kosmos is IYN.
相關臨床試驗
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其他以 EchoNous, Inc. 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。
相關器械（代碼：IYN）
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。
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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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