Konica Minolta Medical Imaging USA announced that the U.S. Food and Drug Administration has cleared the Xpress CR Digital Mammography upgrade for sale.
Wednesday, 02 November 2011 01:00, Written by Tincy
ECRI Institute and the FDA are co-sponsoring a free public conference on the evidence, programs, and implications of patient-centeredness in healthcare on November 29-30, 2011.
Selenia Dimensions is the first commercial mammography system approved to use 2D and 3D (breast tomosynthesis) technologies for breast cancer screening and diagnosis
Mobile devices have made ubiquitous access to patient data a reality for many physicians treating patients at the point of care or on a consultative basis. Yet radiologists have largely remained limited in their ability to use mobile devices for patient care.
Konica Minolta Medical Imaging USA announced that the U.S. Food and Drug Administration has cleared the Xpress CR Digital Mammography upgrade for sale.
New User Interface, Larger Screen Size and Exceptional Image Quality
Selenia Dimensions is the first commercial mammography system approved to use 2D and 3D (breast tomosynthesis) technologies for breast cancer screening and diagnosis
Toshiba Announces FDA Clearance of Extra-Large Knee Array Coil
Mobile devices have made ubiquitous access to patient data a reality for many physicians treating patients at the point of care or on a consultative basis. Yet radiologists have largely remained limited in their ability to use mobile devices for patient care.
