K250299
- 510(k) number
- K250299
- Device name
- CT/ MR Tandem and Ovoid Set
- Applicant
- Varian Medical Systems, Inc. CA · US
- Product code
- JAQ — System, Applicator, Radionuclide, Remote-Controlled
- Decision date
- 2025-05-09
- Date received
- 2025-01-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250299.pdf
Official FDA record: K250299
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.