K233628
- 510(k) number
- K233628
- Device name
- AOS Interstitial Templates, Needles, and Accessories
- Applicant
- Alpha-Omega Services, Inc. CA · US
- Product code
- JAQ — System, Applicator, Radionuclide, Remote-Controlled
- Decision date
- 2024-07-10
- Date received
- 2023-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K233628.pdf
Official FDA record: K233628
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.