K232799
- 510(k) number
- K232799
- Device name
- syngo.via RT Image Suite
- Applicant
- Siemens Medical Solutions USA, Inc. TN · US
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2024-04-26
- Date received
- 2023-09-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232799.pdf
Official FDA record: K232799
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.