K223659
- 510(k) number
- K223659
- Device name
- Jazz
- Applicant
- Ai Medical AG CH
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2023-09-22
- Date received
- 2022-12-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K223659.pdf
Official FDA record: K223659
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.