Computer-aided-detection (CAD) developer iCAD of Nashua, NH, has received U.S. Food and Drug Adminsitration marketing approval for the use of its CAD technology with Denver, CO-based Fischer Imaging’s SenoScan digital mammography system.
The FDA approval expands the firm’s capability to serve both the full field digital mammography and traditional screen film mammography markets, iCAD said.
By AuntMinnie.com staff writersNovember 13, 2003
Related Reading
iCAD posts Q3 results, gets FDA approval, November 6, 2003
iCAD signs U.S. distribution deal, October 16, 2003
iCAD nets Canadian distribution agreement, October 7, 2003
R2 and iCAD bury hatchet, for a price, September 9, 2003
iCAD sales up, losses down for Q2, August 7, 2003
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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)






