K242961
- 510(k) number
- K242961
- Device name
- Intraluminal Applicator Set
- Applicant
- Varian Medical Systems CA · US
- Product code
- JAQ — System, Applicator, Radionuclide, Remote-Controlled
- Decision date
- 2024-11-26
- Date received
- 2024-09-25
- 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: K242961.pdf
Official FDA record: K242961
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.