K252884
- 510(k) number
- K252884
- Device name
- Guided Aarhus Applicator Set
- Applicant
- Varian Medical Systems CA · US
- Product code
- JAQ — System, Applicator, Radionuclide, Remote-Controlled
- Decision date
- 2025-11-19
- Date received
- 2025-09-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252884.pdf
Official FDA record: K252884
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.