Fujifilm Medical Systems USA has received Food and Drug Administration 510(k) clearance to deploy its DryPix dry laser imagers for full-field digital mammography (FFDM) use.
The clearance covers the company’s DryPix 7000, DryPix 5000, and DryPix FM-DP L imagers, according to the Stamford, CT-based vendor.
By AuntMinnie.com staff writersJanuary 15, 2004
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Fujifilm Medical Systems USA, November 18, 2003
Fujifilm nets large VA CR order, November 13, 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)





