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FDA 510(k)

QuickFinder COVID-19/流感抗原自測 / QuickFinder COVID-19/流感抗原專測

K 號：K243262 · 2025-01-13

申請人Osang, LLC
決定日期2025-01-13
產品代碼SCA
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

QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test is the device name listed in this FDA 510(k) record. The listed applicant is Osang, LLC. It received FDA 510(k) clearance on 2025-01-13 under 510(k) number K243262. The device is classified under product code SCA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test?

QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test is a medical device that received FDA 510(k) clearance on 2025-01-13. The listed applicant is Osang, LLC. The 510(k) number is K243262.

When did QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test receive FDA 510(k) clearance?

QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test received FDA 510(k) clearance on 2025-01-13, under 510(k) number K243262.

Who is the listed applicant for QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test?

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

What is the FDA product code for QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test?

The FDA product code for QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test is SCA.

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 Osang, 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。

K241313OHC COVID-19 抗原自測包

相關器械（代碼：SCA）

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。

K261212Flowflex Plus RSV + 流行性感冒A/B + COVID 快速檢測ACON Laboratories, Inc.K251085iHealth 流感A&B/COVID-19/RSV 快速檢測；iHealth 流感A&B/COVID-19/RSV 快速檢測 ProIhealth Labs, Inc.K251092iHealth流感A&B/COVID-19快速檢測; iHealth流感A&B/COVID-19快速檢測ProIhealth Labs, Inc.K251538Status™ COVID-19/流感A&BPrinceton BioMeditech Corp.K251749Flowflex Plus RSV + 流行性感冒A/B + COVID家庭檢測ACON Laboratories, Inc.K251604CareSuperb COVID-19/流感A&B抗原組合居家檢測Access Bio, Inc.

官方來源

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