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.

Clearance details

Applicant: Philips Medical Systems Nederland B.V.
Product code: 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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Data sourced from openFDA. This site is unofficial and independent of the FDA.