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FDA 510(k)

Healgen 快速 COVID-19 抗原檢測

K 號：K232377 · 2024-04-19

申請人Healgen Scientific,, LLC
決定日期2024-04-19
產品代碼QVF
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

Healgen Rapid COVID-19 Antigen Test is the device name listed in this FDA 510(k) record. The listed applicant is Healgen Scientific,, LLC. It received FDA 510(k) clearance on 2024-04-19 under 510(k) number K232377. 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 Healgen Rapid COVID-19 Antigen Test?

Healgen Rapid COVID-19 Antigen Test is a medical device that received FDA 510(k) clearance on 2024-04-19. The listed applicant is Healgen Scientific,, LLC. The 510(k) number is K232377.

When did Healgen Rapid COVID-19 Antigen Test receive FDA 510(k) clearance?

Healgen Rapid COVID-19 Antigen Test received FDA 510(k) clearance on 2024-04-19, under 510(k) number K232377.

Who is the listed applicant for Healgen Rapid COVID-19 Antigen Test?

The FDA 510(k) record lists Healgen Scientific,, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Healgen Rapid COVID-19 Antigen Test?

The FDA product code for Healgen Rapid COVID-19 Antigen Test is QVF.

相關臨床試驗

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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 Healgen Scientific,, 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。

K260095治康快速COVID-19抗原自測包K253705Healgen®精準口腔濾液藥物檢測K252523Healgen®精準口腔濾液藥物檢測COT/THC；Healgen®精準口腔濾液藥物檢測K253567Healgen精準尿液藥物檢測濾卡；Healgen精準家庭尿液藥物檢測濾卡K251800Healgen® URS測試條K251972Healgen® AccuFluor Fentanyl Fluorescence Immunoassay (FIA)測試套件 - 定性；Healgen® 免疫荧光分析儀（OG-H180）

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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

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