下一代NetKonnect
K 號：K220989 · 2022-07-29
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器材摘要
Next Generation NetKonnect is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Digital Health Solutions, Inc.. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K220989. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Next Generation NetKonnect?
Next Generation NetKonnect is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Nihon Kohden Digital Health Solutions, Inc.. The 510(k) number is K220989.
When did Next Generation NetKonnect receive FDA 510(k) clearance?
Next Generation NetKonnect received FDA 510(k) clearance on 2022-07-29, under 510(k) number K220989.
Who is the listed applicant for Next Generation NetKonnect?
The FDA 510(k) record lists Nihon Kohden Digital Health Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Next Generation NetKonnect?
The FDA product code for Next Generation NetKonnect is MHX.
相關臨床試驗
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相關器械（代碼：MHX）
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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