K251577
- 510(k) number
- K251577
- Device name
- LAIA XR
- Applicant
- Augmented Reality Software S.L. ES
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-02-06
- Date received
- 2025-05-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251577.pdf
Official FDA record: K251577
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.