K241764
- 510(k) number
- K241764
- Device name
- Mould Probe MR Safe
- Applicant
- Varian Medical Systems, Inc. CA · US
- Product code
- JAQ — System, Applicator, Radionuclide, Remote-Controlled
- Decision date
- 2025-01-10
- Date received
- 2024-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K241764.pdf
Official FDA record: K241764
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.