Reston Radiology Consultants (Ashburn, Virginia) is a hospital-based imaging practice in business for over twenty years that includes several outpatient centers, including MRI of Reston, where four systems carry an imaging load that reaches a combined average of 24,000 studies annually. This suggests a fair amount of volume seen at that lone

GE Healthcare has received FDA clearance of the Discovery* MR750w wide bore 3.0 Tesla MR system with GEM (Geometry Embracing Method) Suite of Coils.

The U.S. Food and Drug Administration (FDA) has received a citizen petition from the International Contrast Ultrasound Society (ICUS), requesting that the agency remove black box warnings on ultrasound contrast agents.

Diffusion-weighted MRI may be a better determinant than PET-CT of whether lung lesions are cancerous or benign, according to a study conducted by Belgian researchers and presented yesterday at the European Respiratory Society’s Annual Congress in Amsterdam, The Netherlands. The modality could then be used to prevent unnecessary surgery by enabling

MRI safety will be the focus of a two-day public workshop to be held by the U.S. Food and Drug Administration (FDA) on October 25 and October 26.

The American College of Radiology (ACR) is looking for clinical reviewers for its ultrasound accreditation program.

Toshiba today announced that it has received Food and Drug Administration (FDA) clearance for its Vantage Titan™ 3T open-bore MRI scanner.

Microvascular perfusion deficits and reduced arterial perfusion reserve are clearly detectable in patients with peripheral arterial disease (PAD) when dynamic contrast-enhanced ultrasound (CEUS) is used after transient arterial occlusion, report the authors of a feasibility study published online and in the August issue of Investigative Radiology.