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Clinical AI platform for radiology and enterprise imaging workflows.
Last updated: May 25, 2026
Back to directoryFDA-cleared non-invasive plaque analysis software for coronary CTA workflows that reports plaque composition and vessel-level findings.
Cardiology and imaging teams evaluating quantitative CCTA plaque analysis for atherosclerosis risk assessment and treatment planning.
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product-specific source-backed lens: These product-specific signals summarize what the cited sources imply before treating Elucid PlaqueIQ as safe for a local clinical, operational, or research workflow.
| Regulatory / FDA | Match the PlaqueIQ version, 510(k) record, indication, CCTA acquisition requirements, geography, and reimbursement use before adding it to a clinical pathway. |
|---|---|
| Privacy | Review coronary CTA upload, remote access to PHI, encrypted transfer, retention, support access, subcontractors, customer-controller obligations, and DPF or local transfer terms. |
| Evidence | Assess validation for the target CCTA population, scanner/protocol mix, plaque-composition metrics, lesion-level outputs, reader agreement, and downstream treatment or testing decisions. |
| Workflow | Best governed as physician-reviewed coronary CTA plaque analysis feeding structured cardiology risk assessment, prevention, referral, and follow-up workflows. |
Elucid describes PlaqueIQ as FDA-cleared non-invasive plaque analysis based on CCTA and objective histology; FDA materials list PlaqueIQ image-analysis software, while Elucid privacy materials describe PHI handling, remote access, confidentiality, and security controls for medical image processing services.
Not for: Standalone cardiovascular diagnosis, unsupported CTA protocols, or treatment decisions without qualified physician interpretation.
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