FDA 510(k)

MAASTRO 直肠应用器套装

K号: K252717 · 2026-05-20

决定日期2026-05-20

产品代码JAQ

咨询委员会RA

决定实质等同

器械摘要

MAASTRO Rectal 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 2026-05-20 under 510(k) number K252717. 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 MAASTRO Rectal Applicator Set?

MAASTRO Rectal Applicator Set is a medical device that received FDA 510(k) clearance on 2026-05-20. The listed applicant is Varian Medical Systems. The 510(k) number is K252717.

When did MAASTRO Rectal Applicator Set receive FDA 510(k) clearance?

MAASTRO Rectal Applicator Set received FDA 510(k) clearance on 2026-05-20, under 510(k) number K252717.

Who is the listed applicant for MAASTRO Rectal 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 MAASTRO Rectal Applicator Set?

The FDA product code for MAASTRO Rectal 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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