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FDA 510(k)

美國疾病管制局人類流感病毒實時RT-PCR檢測組合：流感A/B分型套件（版本2）；流感A亞型分型套件（版本4）；流感B基因分型套件（版本1.1和2）；以及流感A/H5亞型分型套件（版本4）

K 號：K243274 · 2025-07-11

申請人Centers for Disease Control and Prevention
決定日期2025-07-11
產品代碼OZE
諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)
決定相當於

器材摘要

CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4) is the device name listed in this FDA 510(k) record. The listed applicant is Centers for Disease Control and Prevention. It received FDA 510(k) clearance on 2025-07-11 under 510(k) number K243274. The device is classified under product code OZE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4)?

CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4) is a medical device that received FDA 510(k) clearance on 2025-07-11. The listed applicant is Centers for Disease Control and Prevention. The 510(k) number is K243274.

When did CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4) receive FDA 510(k) clearance?

CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4) received FDA 510(k) clearance on 2025-07-11, under 510(k) number K243274.

Who is the listed applicant for CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4)?

The FDA 510(k) record lists Centers for Disease Control and Prevention as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4)?

The FDA product code for CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A SubTyping Kit (VER 4); Influenza B Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4) is OZE.

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 Centers for Disease Control and Prevention 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。

K260812弗朗西斯菌屬實時PCR檢測試劑K252072弗朗西斯菌屬實時PCR檢測試劑K243931美國疾病管制局人類流感病毒實時RT-PCR檢測組合：流感A/B分型套件（版本2）；流感A亞型分型套件（版本4）；流感B系統發育基因分型套件（版本1.1和2）；以及流感A/H5亞型分型套件（版本4）K241110美國疾病管制局人類流感病毒實時RT-PCR檢測組合，流感A型亞型分類套件（Ver4）K222558非天花正痘病毒實時PCR引物及探針組K221834非天花正痘病毒實時PCR引物及探針組

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相關器械（代碼：OZE）

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。

K243931美國疾病管制局人類流感病毒實時RT-PCR檢測組合：流感A/B分型套件（版本2）；流感A亞型分型套件（版本4）；流感B系統發育基因分型套件（版本1.1和2）；以及流感A/H5亞型分型套件（版本4）Centers for Disease Control and PreventionK241110美國疾病管制局人類流感病毒實時RT-PCR檢測組合，流感A型亞型分類套件（Ver4）Centers for Disease Control and PreventionK230236麗拉A+B型流感檢測試劑Quidel CorporationK220801ID Now儀器，ID Now A型及B型流感2，ID NOW 链球菌A 2Abbott Diagnostics Scarborough, Inc.K200370美國疾病管制局人類流感病毒實時RT-PCR診斷組合，流感A/B分型套件，美國疾病管制局人類流感病毒實時RT-PCR診斷組合，流感A亞型分型套件，美國疾病管制局人類流感病毒實時RT-PCR，流感A/H5亞型分型套件Centers for Disease Control and PreventionK182513FluChip-8G 間接流感A+B檢測試劑Indevr, Inc.

官方來源

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