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FDA 510(k)

Acucy®流感A&B测试与Acucy® 2系统

K号: K241188 · 2025-04-18

决定日期2025-04-18
产品代码PSZ
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器械摘要

Acucy® Influenza A&B Test with the Acucy® 2 System is the device name listed in this FDA 510(k) record. The listed applicant is SEKISUI Diagnostics, LLC. It received FDA 510(k) clearance on 2025-04-18 under 510(k) number K241188. The device is classified under product code PSZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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

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

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