K242275
- 510(k) number
- K242275
- 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
- 2024-08-30
- Date received
- 2024-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K242275.pdf
Official FDA record: K242275
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.