K232000
- 510(k) number
- K232000
- Device name
- syngo.via MI Workflows; Scenium; syngo MBF
- Applicant
- Siemens Medical Solutions USA, Inc. IL · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2023-11-28
- Date received
- 2023-07-05
- 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: K232000.pdf
Official FDA record: K232000
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.