烏拉素氮含量2
K 號：K203771 · 2022-05-31
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器材摘要
Urea Nitrogen2 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Ireland Diagnostics Division. It received FDA 510(k) clearance on 2022-05-31 under 510(k) number K203771. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Urea Nitrogen2?
Urea Nitrogen2 is a medical device that received FDA 510(k) clearance on 2022-05-31. The listed applicant is Abbott Ireland Diagnostics Division. The 510(k) number is K203771.
When did Urea Nitrogen2 receive FDA 510(k) clearance?
Urea Nitrogen2 received FDA 510(k) clearance on 2022-05-31, under 510(k) number K203771.
Who is the listed applicant for Urea Nitrogen2?
The FDA 510(k) record lists Abbott Ireland Diagnostics Division as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Urea Nitrogen2?
The FDA product code for Urea Nitrogen2 is CDQ.
相關臨床試驗
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其他以 Abbott Ireland Diagnostics Division 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。
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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