FDA 510(k)

多模态模拟工作空间（MM Sim）(v1.0.0)

K号: K260207 · 2026-05-27

申请人Philips Medical Systems Nederland B.V.

决定日期2026-05-27

产品代码MUJ

咨询委员会RA

决定实质等同

器械摘要

Multimodality Simulation Workspace (MM Sim) (v1.0.0) is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2026-05-27 under 510(k) number K260207. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Multimodality Simulation Workspace (MM Sim) (v1.0.0)?

Multimodality Simulation Workspace (MM Sim) (v1.0.0) is a medical device that received FDA 510(k) clearance on 2026-05-27. The listed applicant is Philips Medical Systems Nederland B.V.. The 510(k) number is K260207.

When did Multimodality Simulation Workspace (MM Sim) (v1.0.0) receive FDA 510(k) clearance?

Multimodality Simulation Workspace (MM Sim) (v1.0.0) received FDA 510(k) clearance on 2026-05-27, under 510(k) number K260207.

Who is the listed applicant for Multimodality Simulation Workspace (MM Sim) (v1.0.0)?

FDA 510(k)记录中列出Philips Medical Systems Nederland B.V.为申请人。这本身并不足以确定该设备的制造商。

What is the FDA product code for Multimodality Simulation Workspace (MM Sim) (v1.0.0)?

The FDA product code for Multimodality Simulation Workspace (MM Sim) (v1.0.0) is MUJ.

列明Philips Medical Systems Nederland B.V.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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