K260217
- 510(k) number
- K260217
- Device name
- AI Platform 2.2 (AIP002)
- Applicant
- Exo Imaging CA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-02-24
- Date received
- 2026-01-23
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260217.pdf
Official FDA record: K260217
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.