K241876
- 510(k) number
- K241876
- Device name
- Vitesse (5.0)
- Applicant
- Varian Medical Systems CA · US
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2024-10-23
- Date received
- 2024-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K241876.pdf
Official FDA record: K241876
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.