K253962
- 510(k) number
- K253962
- Device name
- ClearCheck (RADCC V2.7)
- Applicant
- Radformation, Inc. NY · US
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2026-04-03
- Date received
- 2025-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K253962.pdf
Official FDA record: K253962
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.