Philips EPIQ Inspira and Affiniti ultrasound cleared by FDA
FDA cleared Philips' EPIQ Inspira and Affiniti diagnostic ultrasound systems via 510(k) pathway (product code IYN).
FDA cleared Philips' EPIQ Inspira and Affiniti diagnostic ultrasound systems via 510(k) pathway (product code IYN).
FDA grants 510(k) clearance to Siemens' syngo.CT Brain Quantification, a software device for quantification of brain CT images.
Samsung Medison has received FDA 510(k) clearance for its family of EVO diagnostic ultrasound systems, including X, XP, and XC models.
Among 243 thoracic CTs, 10% had incorrect pulmonary nodule management recommendations (more common from general radiologists). Automated triage triggering review when AI missed a reported nodule was the most cost-saving pathway per corrected error.
Digital 3D modeling aids preoperative planning, multidisciplinary communication, and training in pediatric surgical oncology, but clinical outcome evidence is lacking. An expert white paper calls for progress through AI integration, multicenter validation, centralized digital tw…
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Thoracic Aorta - Chronic dilatation
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