FDA 510(k)

3mensio Workstation

K号: K250330 · 2025-11-03

决定日期2025-11-03

产品代码QIH

咨询委员会RA

决定实质等同

器械摘要

3mensio Workstation is the device name listed in this FDA 510(k) record. The listed applicant is Pie Medical Imaging BV. It received FDA 510(k) clearance on 2025-11-03 under 510(k) number K250330. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the 3mensio Workstation?

3mensio Workstation is a medical device that received FDA 510(k) clearance on 2025-11-03. The listed applicant is Pie Medical Imaging BV. The 510(k) number is K250330.

When did 3mensio Workstation receive FDA 510(k) clearance?

3mensio Workstation received FDA 510(k) clearance on 2025-11-03, under 510(k) number K250330.

Who is the listed applicant for 3mensio Workstation?

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

What is the FDA product code for 3mensio Workstation?

The FDA product code for 3mensio Workstation is QIH.

列明Pie Medical Imaging BV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。

K232147CAAS 工作站 K232007CAAS MR 解决方案 K212376Caas Qardia K181825CAAS MR 解决方案 K180019CAAS 工作站 K162376CAAS MR 4D 流

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