CDM Insights
K 號：K240680 · 2024-12-06
廣告
器材摘要
CDM Insights is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Brain Diagnostics, Ltd.. It received FDA 510(k) clearance on 2024-12-06 under 510(k) number K240680. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CDM Insights?
CDM Insights is a medical device that received FDA 510(k) clearance on 2024-12-06. The listed applicant is Oxford Brain Diagnostics, Ltd.. The 510(k) number is K240680.
When did CDM Insights receive FDA 510(k) clearance?
CDM Insights received FDA 510(k) clearance on 2024-12-06, under 510(k) number K240680.
Who is the listed applicant for CDM Insights?
The FDA 510(k) record lists Oxford Brain Diagnostics, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CDM Insights?
The FDA product code for CDM Insights is QIH.
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。
相關器械（代碼：QIH）
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。
廣告