Multimodality Simulation Workspace (MM Sim) (v1.0.0)— 510(k) K260207

Name: FDA 510(k) clearance K260207
Creator: U.S. Food and Drug Administration
Published: 2026-05-27

Substantially Equivalent

Philips Medical Systems Nederland B.V.

FDA 510(k) clearance K260207 for Multimodality Simulation Workspace (MM Sim) (v1.0.0), Substantially Equivalent on 2026-05-27. Applicant: Philips Medical Systems Nederland B.V.. Device class: 2.

Summary

Philips Medical Systems Nederland's Multimodality Simulation Workspace (MM Sim), listed as v1.0.0, is filed under MUJ, radiation therapy treatment planning systems.

Class II, 21 CFR 892.5050. Radiology is both the classification panel and the review panel. It was a Traditional 510(k).

Philips filed from Best, Netherlands. Review took 124 calendar days (January 23 to May 27, 2026).

Clearance details

Applicant: Philips Medical Systems Nederland B.V.
Product code: Product code MUJ
Device class: Class 2
Regulation: 21 CFR 892.5050
Advisory panel: Radiology
Date received: 2026-01-23
Decision date: 2026-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Best, NL

Download summary PDF View on FDA.gov ↗

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