Applied Biosystems™ TaqPath™ COVID-19 诊断PCR試劑套件
K 號:K233453 · 2024-07-10
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器材摘要
常見問題
What is the Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit?
Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit is a medical device that received FDA 510(k) clearance on 2024-07-10. The listed applicant is Life Technologies Corporation. The 510(k) number is K233453.
When did Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit receive FDA 510(k) clearance?
Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit received FDA 510(k) clearance on 2024-07-10, under 510(k) number K233453.
Who is the listed applicant for Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit?
The FDA 510(k) record lists Life Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit?
The FDA product code for Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit is QQX.
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其他以 Life Technologies Corporation 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:QQX)
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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