WELLlife 流感A&B家用检测仪;WELLlife 流感A&B检测仪
K号: K251563 · 2025-08-20
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器械摘要
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
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。
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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