K232899
- 510(k) number
- K232899
- Device name
- AI-Rad Companion Organs RT
- Applicant
- Siemens Medical Solutions U.S.A. PA · US
- Product code
- QKB — Radiological Image Processing Software For Radiation
- Decision date
- 2024-04-03
- Date received
- 2023-09-18
- 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: K232899.pdf
Official FDA record: K232899
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.