syngo.via MI Workflows; Scenium; syngo MBF— 510(k) K232000
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K232000 for syngo.via MI Workflows; Scenium; syngo MBF, Substantially Equivalent on 2023-11-28. Applicant: Siemens Medical Solutions USA, Inc..
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hoffman Estates, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.