FDA 510(k)

引导阿胡斯应用器套装

K号: K252884 · 2025-11-19

决定日期2025-11-19

产品代码JAQ

咨询委员会RA

决定实质等同

器械摘要

Guided Aarhus Applicator Set is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems. It received FDA 510(k) clearance on 2025-11-19 under 510(k) number K252884. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Guided Aarhus Applicator Set?

Guided Aarhus Applicator Set is a medical device that received FDA 510(k) clearance on 2025-11-19. The listed applicant is Varian Medical Systems. The 510(k) number is K252884.

When did Guided Aarhus Applicator Set receive FDA 510(k) clearance?

Guided Aarhus Applicator Set received FDA 510(k) clearance on 2025-11-19, under 510(k) number K252884.

Who is the listed applicant for Guided Aarhus Applicator Set?

The FDA 510(k) record lists Varian Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Guided Aarhus Applicator Set?

The FDA product code for Guided Aarhus Applicator Set is JAQ.

列明Varian Medical Systems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。

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