FDA 510(k)

CT/ MR 连续和椭圆形套装

K号: K250299 · 2025-05-09

决定日期2025-05-09

产品代码JAQ

咨询委员会RA

决定实质等同

器械摘要

CT/ MR Tandem and Ovoid Set is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2025-05-09 under 510(k) number K250299. 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 CT/ MR Tandem and Ovoid Set?

CT/ MR Tandem and Ovoid Set is a medical device that received FDA 510(k) clearance on 2025-05-09. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K250299.

When did CT/ MR Tandem and Ovoid Set receive FDA 510(k) clearance?

CT/ MR Tandem and Ovoid Set received FDA 510(k) clearance on 2025-05-09, under 510(k) number K250299.

Who is the listed applicant for CT/ MR Tandem and Ovoid Set?

FDA 510(k)记录中列出Varian Medical Systems, Inc.为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for CT/ MR Tandem and Ovoid Set?

The FDA product code for CT/ MR Tandem and Ovoid Set is JAQ.

列明Varian Medical Systems, Inc.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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