FDA 510(k)

GenaCheck COVID-19 快速自測包

K 號：K251753 · 2025-09-05

決定日期2025-09-05

產品代碼QYT

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

GenaCheck COVID-19 Rapid Self-Test is the device name listed in this FDA 510(k) record. The listed applicant is Genabio Diagnostics, Inc.. It received FDA 510(k) clearance on 2025-09-05 under 510(k) number K251753. The device is classified under product code QYT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the GenaCheck COVID-19 Rapid Self-Test?

GenaCheck COVID-19 Rapid Self-Test is a medical device that received FDA 510(k) clearance on 2025-09-05. The listed applicant is Genabio Diagnostics, Inc.. The 510(k) number is K251753.

When did GenaCheck COVID-19 Rapid Self-Test receive FDA 510(k) clearance?

GenaCheck COVID-19 Rapid Self-Test received FDA 510(k) clearance on 2025-09-05, under 510(k) number K251753.

Who is the listed applicant for GenaCheck COVID-19 Rapid Self-Test?

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

What is the FDA product code for GenaCheck COVID-19 Rapid Self-Test?

The FDA product code for GenaCheck COVID-19 Rapid Self-Test is QYT.

其他以 Genabio Diagnostics, Inc. 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。

K240545GenaCheck™ 硅膠無粉檢查手套，適用於與化學治療藥物及芬太尼鹽酸（XS/S/M/L/XL）使用之檢驗。

相關器械（代碼：QYT）

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。

K260754Fastep COVID-19 抗原筆式家庭檢測；Fastep COVID-19 抗原筆式檢測Assure Tech., LLC K260095治康快速COVID-19抗原自測包Healgen Scientific,, LLC K251916GenBody COVID-19 Ag 家庭檢測Genbody.Inc.K251595COVID-19 快速自測檢測器InBios International, Inc.K241313OHC COVID-19 抗原自測包Osang, LLC K243518BinaxNOW™ COVID-19 抗原自測包Abbott Diagnostics Scarborough, Inc.

官方來源

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