K240953
- 510(k) number
- K240953
- Device name
- AI Platform 2.0 (AIP002)
- Applicant
- Exo Imaging CA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-08-05
- Date received
- 2024-04-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K240953.pdf
Official FDA record: K240953
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.