The Food and Drug Administration has authorized the American College of Radiology to serve as the official accreditation agency for Fischer Imaging’s SenoScan full-field digital mammography (FFDM) system. Previously, SenoScan users had to file for accreditation directly with the FDA, according to Denver-based Fischer.
Fischer said that ACR registration, effective August 15, will allow for a more streamlined accreditation process, and eliminate the U.S government’s requirement for SenoScan users to also have a separate film-screen mammography unit available.
By AuntMinnie.com staff writers
August 18, 2003
Related Reading
Fischer, Philips to develop mammo/US prototype, August 12, 2003
Fischer goes direct in Europe, August 5, 2003
Fischer offers restated results, July 17, 2003
Fischer responds to SEC inquiry, June 12, 2003
Fischer delays filing Q1 results, May 15, 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)






