聯盟 NES 流感 A/B、RSV 及 COVID-19
K 號：K251978 · 2025-12-23
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器材摘要
LIAISON NES FLU A/B, RSV & COVID-19 is the device name listed in this FDA 510(k) record. The listed applicant is Diasorin Molecular, LLC. It received FDA 510(k) clearance on 2025-12-23 under 510(k) number K251978. The device is classified under product code QOF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LIAISON NES FLU A/B, RSV & COVID-19?
LIAISON NES FLU A/B, RSV & COVID-19 is a medical device that received FDA 510(k) clearance on 2025-12-23. The listed applicant is Diasorin Molecular, LLC. The 510(k) number is K251978.
When did LIAISON NES FLU A/B, RSV & COVID-19 receive FDA 510(k) clearance?
LIAISON NES FLU A/B, RSV & COVID-19 received FDA 510(k) clearance on 2025-12-23, under 510(k) number K251978.
Who is the listed applicant for LIAISON NES FLU A/B, RSV & COVID-19?
The FDA 510(k) record lists Diasorin Molecular, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIAISON NES FLU A/B, RSV & COVID-19?
The FDA product code for LIAISON NES FLU A/B, RSV & COVID-19 is QOF.
相關臨床試驗
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其他以 Diasorin Molecular, LLC 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：QOF）
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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