K252784
- 510(k) number
- K252784
- Device name
- eXaSkin Plus
- Applicant
- Anatomical Geometry S.L. ES
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2026-05-22
- Date received
- 2025-09-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K252784.pdf
Official FDA record: K252784
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.