K250289
- 510(k) number
- K250289
- Device name
- Intracavitary/Interstitial System
- Applicant
- Varian Medical Systems CA · US
- Product code
- JAQ — System, Applicator, Radionuclide, Remote-Controlled
- Decision date
- 2025-04-25
- Date received
- 2025-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K250289.pdf
Official FDA record: K250289
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.