K252258
- 510(k) number
- K252258
- Device name
- VERIQA RT EPID 3D
- Applicant
- Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla DE
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2026-04-15
- Date received
- 2025-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K252258.pdf
Official FDA record: K252258
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.