K260207
- 510(k) number
- K260207
- Device name
- Multimodality Simulation Workspace (MM Sim) (v1.0.0)
- Applicant
- Philips Medical Systems Nederland B.V. NL
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2026-05-27
- Date received
- 2026-01-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K260207.pdf
Official FDA record: K260207
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.