K233622
- 510(k) number
- K233622
- Device name
- AlignRT Plus
- Applicant
- Vision Rt, Ltd. GB
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2024-03-29
- Date received
- 2023-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K233622.pdf
Official FDA record: K233622
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.