BD Veritor 系統快速檢測 SARS-CoV-2
K 號：K243872 · 2025-06-16
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器材摘要
BD Veritor System for SARS-CoV-2 is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-06-16 under 510(k) number K243872. The device is classified under product code QVF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BD Veritor System for SARS-CoV-2?
BD Veritor System for SARS-CoV-2 is a medical device that received FDA 510(k) clearance on 2025-06-16. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K243872.
When did BD Veritor System for SARS-CoV-2 receive FDA 510(k) clearance?
BD Veritor System for SARS-CoV-2 received FDA 510(k) clearance on 2025-06-16, under 510(k) number K243872.
Who is the listed applicant for BD Veritor System for SARS-CoV-2?
The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Veritor System for SARS-CoV-2?
The FDA product code for BD Veritor System for SARS-CoV-2 is QVF.
相關臨床試驗
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其他以 Becton, Dickinson and Company 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：QVF）
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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