Acucy®流感A&B测试与Acucy® 2系统
K号: K241188 · 2025-04-18
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器械摘要
常见问题
What is the Acucy® Influenza A&B Test with the Acucy® 2 System?
Acucy® Influenza A&B Test with the Acucy® 2 System is a medical device that received FDA 510(k) clearance on 2025-04-18. The listed applicant is SEKISUI Diagnostics, LLC. The 510(k) number is K241188.
When did Acucy® Influenza A&B Test with the Acucy® 2 System receive FDA 510(k) clearance?
Acucy® Influenza A&B Test with the Acucy® 2 System received FDA 510(k) clearance on 2025-04-18, under 510(k) number K241188.
Who is the listed applicant for Acucy® Influenza A&B Test with the Acucy® 2 System?
The FDA 510(k) record lists SEKISUI Diagnostics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Acucy® Influenza A&B Test with the Acucy® 2 System?
The FDA product code for Acucy® Influenza A&B Test with the Acucy® 2 System is PSZ.
相关临床试验
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列明SEKISUI Diagnostics, LLC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:PSZ)
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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