K232479
- 510(k) number
- K232479
- Device name
- ART-Plan
- Applicant
- Therapanacea FR
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2023-12-22
- Date received
- 2023-08-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K232479.pdf
Official FDA record: K232479
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.