April 15, 2014 — Mevion Medical Systems announced an agreement with Chiyoda Technol Corp. for the exclusive distribution of the Mevion S250 proton therapy system in the Japanese market.

April 15, 2014 — Shimadzu Medical Systems USA announced an agreement with Konica Minolta Medical Imaging to expand the availability of the AeroDR portable wireless solution to MobileArt portable X-ray systems.

aycan, in conjunction with its business partner, medQ,announced the availability of aycan workflow, a fully integrated radiology information system/picture archive and communication system (RIS/PACS) solution that provides a turnkey end-to-end digital imaging and patient management system.

The U.S. Food and Drug Administration (FDA) granted 510(k) market clearance for the GE Healthcare Revolution computed tomography (CT) system. The 256-slice CT system offers technology that provides excellent image quality and clinical capabilities through the convergence of coverage, spatial resolution and temporal resolution.
 

April 15, 2014 — VuComp Inc. announced it has released an updated version of its M-Vu Breast Density technology. The new M-Vu Breast Density 2.0 adds a critical dimension to the analysis of dense breast tissue. The VuComp density category, analogous to the BI-RADS breast density composition category, is now correlated to not only the amount, but also the distribution – the actual dispersion – of fibroglandular tissue.

April 11, 2014 — A University of Colorado Cancer Center study presented at the 2014 annual meeting of the American Association for Cancer Research (AACR) describes a novel method to "manipulate the lipid metabolism in the cancer cell to trick them to use more radiolabeled glucose, the basis of PET [positron emission tomography] scanning," according to Isabel Schlaepfer, Ph.D., investigator at the CU Cancer Center Department of Pharmacology and recipient of a 2014 Minority Scholar Award in Cancer Research from AACR.

April 11, 2014 — Calgary Scientific Inc. announced their latest Class II clearance from the U.S. Food and Drug Administration (FDA). Its enterprise image-viewing solution, ResolutionMD, is now cleared for diagnosis on mobile devices for all imaging modalities. This builds upon their previous clearances for diagnosis using web, iOS and Android devices.

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