K242551
- 510(k) number
- K242551
- Device name
- syngo Dynamics (Version VA41D)
- Applicant
- Siemens Healthcare GmbH DE
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-04-03
- Date received
- 2024-08-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K242551.pdf
Official FDA record: K242551
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.