K233331
- 510(k) number
- K233331
- Device name
- MediOMx
- Applicant
- Pmx, Inc. IL · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-06-17
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 3.9 MB · U.S. public domain
Also available from FDA: K233331.pdf
Official FDA record: K233331
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.