K252304
- 510(k) number
- K252304
- Device name
- syngo.via RT Image Suite VC10
- Applicant
- Varian Medical Systems, Inc. CA · US
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2026-03-18
- Date received
- 2025-07-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K252304.pdf
Official FDA record: K252304
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.