The Food and Drug Administration has rescheduled its radiological devices advisory panel meeting to review Computerized Thermal Imaging’s breast imaging system. According to the Lake Oswego, OR-based developer, the panel meeting will be held December 10 in Gaithersburg, MD. The panel will discuss and make recommendations regarding the manufacturer’s premarket approval application for the product.
AuntMinnie.com staff writersOctober 16, 2002
Related Reading
CTI BCS 2100 slated for FDA panel review, July 25, 2002
CTI faces shareholder lawsuits, May 15, 2002
CTI to receive $22.5 million in financing, December 21, 2001
CTI begins in-house manufacturing, August 15, 2001
CTI signs on four distributors, August 9, 2001
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![A normal mammogram confirmed by three-year radiologic follow-up illustrates reader-marked regions of interest (ROIs) during (A) unaided (round 1) and (B) artificial intelligence (AI)–assisted (round 2) reading. Each colored dot represents an ROI for recall by a human reader. Readers could mark more than one ROI per case, represented by multiple dots of the same color. During AI-assisted reading, the AI system displayed three visible prompts: two with suspicion of malignancy scores of 35% (left mediolateral oblique [L MLO] and craniocaudal [L CC]) and one with a suspicion of malignancy score of 10% (right craniocaudal [R CC]), shown as polygonal overlays. Without AI, six of 10 readers (60%) marked a false-positive ROI. With AI assistance, this fell to two of 10 (20%). R MLO = right mediolateral oblique.](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/07/2026-07-14-radiology-mammogram-ai-auto-bias.H0bYO8QlWs.jpg?auto=format%2Ccompress&fit=crop&h=112&q=70&w=112)






