Fujifilm Medical Systems USA has received clearance from the U.S. Food and Drug Administration (FDA) for its portable digital x-ray system, the company reported.
Fuji Computed Radiography (FCR) Go includes the same processing features available at the fixed technologist workstation and FCR digital x-ray cassette reader in an imaging department, according to Fuji. The device accommodates wireless or hardwired connection to a facility's network and features Fuji's SpeedLink X-ray Control Software, according to the Stamford, CT-based vendor.
Related Reading
Fuji promotes mammograms in NYC, May 12, 2008
Fuji donates two FFDM systems, May 1, 2008
Fuji awards ARRS grants, April 22, 2008
FDA OKs iCAD SecondLook with Fuji FCRm, April 7, 2008
Fuji hits FCRm milestone, March 31, 2008
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![Representative example of a 16-year-old male patient with underlying X-linked adrenoleukodystrophy. (A, B) Paired anteroposterior (AP) chest radiograph and dual-energy x-ray absorptiometry (DXA) report shows lumbar spine (L1 through L4) areal bone mineral density (BMD). The DXA report was reformatted for anonymization and improved readability. The patient had low BMD (Z score ≤ −2.0). (C) Model (chest radiography [CXR]–BMD) output shows the predicted raw BMD and Z score in comparison with the DXA reference standard, together with interpretability analyses using Shapley additive explanations (SHAP) and gradient-weighted class activation maps. The patient was classified as having low BMD, consistent with the reference standard. AM = age-matched, DEXA = dual-energy x-ray absorptiometry, RM2 = room 2, SNUH = Seoul National University Hospital, YA = young adult.](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/04/ai-children-bone-density.0snnf2EJjr.jpg?auto=format%2Ccompress&fit=crop&h=112&q=70&w=112)



