K251199
- 510(k) number
- K251199
- Device name
- Allia Moveo
- Applicant
- GE Medical Systems SCS FR
- Product code
- OWB — Interventional Fluoroscopic X-Ray System
- Decision date
- 2025-12-09
- Date received
- 2025-04-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K251199.pdf
Official FDA record: K251199
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.