Women's imaging vendor Hologic has received U.S. Food and Drug Administration (FDA) approval for its R2 DigitalNow HD software, designed to process digitized film-screen mammograms for comparison.
The software adapts each digitized film image to a selected contrast and tissue intensity that models a digital mammography system, according to the Bedford, MA-based vendor. It also embeds a series of lookup tables in the image that allow Integrating the Healthcare Enterprise (IHE) mammography-conformant workstations to draw out less evident regions of density within digitized films, Hologic said.
Related Reading
Hologic posts large loss in Q2, delays tomo review, May 5, 2009
Hologic completes Netherlands contract, March 6, 2009
Hologic grows revenue in fiscal Q1, February 3, 2009
Hologic expects Q1 revenue shortfall, January 12, 2009
Hologic posts mixed year-end results, November 12, 2008
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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)






