K260750
- 510(k) number
- K260750
- Device name
- Virtual Cone (1.0)
- Applicant
- Varian Medical Systems, Inc. CA · US
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2026-07-08
- Date received
- 2026-03-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K260750.pdf
Official FDA record: K260750
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.