K232489
- 510(k) number
- K232489
- Device name
- VenusX
- Applicant
- Linatech, LLC CA · US
- Product code
- IYE — Accelerator, Linear, Medical
- Decision date
- 2024-04-12
- Date received
- 2023-08-17
- 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: K232489.pdf
Official FDA record: K232489
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.