K232744
- 510(k) number
- K232744
- Device name
- syngo Virtual Cockpit (VB10A)
- Applicant
- Siemens Healthcare GmbH DE
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2023-12-21
- Date received
- 2023-09-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K232744.pdf
Official FDA record: K232744
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.