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FDA 510(k)

WELLlife 流感A&B家用检测仪;WELLlife 流感A&B检测仪

K号: K251563 · 2025-08-20

决定日期2025-08-20
产品代码SCA
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器械摘要

WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test is the device name listed in this FDA 510(k) record. The listed applicant is Wondfo USA Co, Ltd.. It received FDA 510(k) clearance on 2025-08-20 under 510(k) number K251563. The device is classified under product code SCA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test?

WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test is a medical device that received FDA 510(k) clearance on 2025-08-20. The listed applicant is Wondfo USA Co, Ltd.. The 510(k) number is K251563.

When did WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test receive FDA 510(k) clearance?

WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test received FDA 510(k) clearance on 2025-08-20, under 510(k) number K251563.

Who is the listed applicant for WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test?

The FDA 510(k) record lists Wondfo USA Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test?

The FDA product code for WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test is SCA.

相关临床试验

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列明Wondfo USA Co, Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

相关器械(代码:SCA)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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