C4 Imaging LLC announced U.S. Food and Drug Administration (FDA) 510(k) clearance of its first product, the Sirius MRI Marker.
The Radiation Therapy Alliance (RTA), a nonprofit organization representing 227 community-based radiation therapy centers, commended the Centers for Medicare and Medicaid Services (CMS) for withdrawing the proposal to cap certain freestanding radiation oncology reimbursements at the OPD/ASC rates in the CY 2014 Physician Fee Schedule Final Rule, issued Nov. 27.
Using a compact but powerful laser, a research team at the University of Nebraska-Lincoln has developed a new way to generate synchrotron X-rays.
eHealth Saskatchewan plays a vital role in providing IT services to patients, health care providers, and partners such ...
The U.S. Centers for Medicare & Medicaid Services (CMS) finalized updates to payment policies and payment rates for services furnished under the Medicare Physician Fee Schedule (MPFS) on or after Jan. 1, 2014.
Women with interruptions in health insurance coverage or with low income levels had a significantly increased likelihood of failing to receive breast cancer care that is in concordance with recommended treatment guidelines, according to results presented here at the Sixth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved, held Dec. 6-9.

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Previous evidence, including published National Lung Cancer Screening Trial (NLST) results, shows that computed tomography (CT) lung cancer screening significantly reduces lung cancer deaths in high risk patients*, and is appropriate, with careful patient selection and follow-up. This benefit significantly outweighs the comparatively modest rate of overdiagnosis noted in an article published online Dec. 9 in JAMA Internal Medicine. The American College of Radiology (ACR) will continue guideline and appropriateness criteria creation to support CT lung cancer screening programs across the country.
While most women understand the importance of health screenings, an estimated 72 million have missed or postponed a ...
TomTec Imaging Systems GmbH announced the U.S. Food and Drug Administration (FDA) 510(k) clearance for its new TomTec-Arena software solution.
GE Healthcare showcased several new offerings that enable low-dose imaging procedures and help clinicians track and measure dose at the Radiological Society of North America Annual Meeting (RSNA 2013).
Konica Minolta Medical Imaging announced that its parent company, Konica Minolta, Inc., has signed a business transfer agreement with Panasonic Healthcare Co., Ltd. (Panasonic Healthcare) under which the ultrasonic diagnostic equipment business of Panasonic Healthcare is to be transferred to Konica Minolta. All Panasonic Healthcare's assets necessary for planning, development, manufacturing, sales, maintenance, etc., will be transferred, effective on January 1, 2014.
Fujifilm’s APERTO Lucent is a 0.4T mid-field, open MRI system addressing today’s capability and image quality needs ...
Hear why Siemens SOMATOM Definition Edge is the CT your emergency department (ED) has been dreaming about from the ...
OR Technology announced it has received U.S. Food and Drug Administration (FDA) clearance for the combination of OR Technology dicomPACSDX-R acquisition and diagnostic software with different digital radiography (DR) detectors for X-ray images in the human medicine.
American Shared Hospital Services, a provider of turnkey technology solutions for advanced radiosurgical and radiation therapy services, announced that the Centers for Medicare and Medicaid Services (CMS) has posted its final Medicare hospital outpatient prospective payment rates for calendar year 2014.
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Fujifilm Medical Systems USA Inc. announced U.S Food and Drug Administration (FDA) 510(k) clearance of its Gadolinium and Cesium digital X-ray detectors for pediatric use.
3M Health Information Systems released 3M ChartScriptMD Software for Radiology, a reporting application that makes it easy for busy radiologists to create, sign and distribute complete reports and communicate diagnostic findings all from a single integrated system.
NEC Display Solutions of America, a provider of commercial LCD display and projector solutions, announced the U.S. Food and Drug Administration (FDA) 510(k) market clearance of the 24-inch MultiSync MD242C2 referral-grade, widescreen display for diagnostic review applications in healthcare organizations.
GE Healthcare announced at the Radiological Society of North America Annual Meeting (RSNA 2013) the launch of Centricity 360, a GE Predictivity solution.
Konica Minolta Medical Imaging announced the launch of the Sonimage P3 hand-held ultrasound device. The Sonimage P3 brings advanced imaging capabilities to the patient or bedside.
GE Healthcare announced at the Radiological Society of North America Annual Meeting (RSNA 2013) in Chicago that its U.S. Food and Drug Administration (FDA) 510(k)-pending Revolution CT 256-slice system has captured a motion-free image of the human heart in just one beat.
Siemens Healthcare introduced an angiography system optimized for broad clinical utilization at the Radiological Society of North America Annual Meeting (RSNA 2013).
Over the past decade, medical imaging has gone from being one of the fastest growing categories of Medicare spending to one of the slowest relative to other Medicare services, according to a new study.