News

Healthcare organizations looking to implement low dose protocols for computed tomography (CT) exams on all scanners, regardless of disparate locations, can now benefit from SafeCT ...

Infinitt North America will be featuring Dose M 2.0 radiation dose tracking software at this year’s RSNA in Chicago. The new version expands the capture of dose data from multiple-modalities and...

Calgary Scientific Inc. has gained U.S. Food and Drug Administration (FDA) clearance of ResolutionMD 4.0 diagnostic medical imaging software for all modalities and China Food and Drug...

Siemens FDA Clearance ACUSON SC2000 Prime Ultrasound System

Siemens Healthcare has announced that the U.S. Food and Drug Administration (FDA) has cleared the new Prime edition of its Acuson SC2000 premium cardiovascular imaging system — a system that...

October 20, 2014 — Sony Electronics’ Medical Systems Division is highlighting four new medical printers at RSNA 2014: models UP-D898MD, UP-X898MD, UP-991AD and UP-...

Accolade pacemaker, Ingevity lead, Boston Scientific

Boston Scientific Corp. has received CE mark approval for the Accolade pacemaker family. 

Samsung Tablet-based Ultrasound Clinical, PT60A

Samsung Electronics America Inc. announced the preliminary results of a groundbreaking trial into the use of tablet-based ultrasound in emergency services vehicles.

Medtronic FDA Approval CapSureFix Novus MRI SureScan 5076 Lead

Medtronic announced the U.S. Food and Drug Administration (FDA) approval of its CapSureFix Novus MRI SureScan 5076 Lead for use with magnetic resonance imaging (MRI). 

Imricor Medical Systems Inc. announced that it has entered into a license agreement with Sorin Group to develop magnetic resonance imaging (MRI) compatible leads for use with...

Imricor Medical Systems, Inc. announced the first three cardiac ablation procedures were completed in the first clinical study that is evaluating the feasibility of their magnetic resonance (MR)-...

October 15, 2014 — Imaging can be a cost-effective way to identify people at risk for stroke who might benefit from aggressive intervention, according to a new modeling study published online in...

The U.S. Food and Drug Administration (FDA) approved Lumason (sulfur hexafluoride lipid microsphere) for patients whose ultrasound image of the heart (echocardiograms) are hard to see with...

Although cardiovascular disease is largely avoidable through lifestyle modifications, it remains the nation’s number one cause of death. While annual wellness exams offer physicians the chance to...

This webinar will discuss why contemporary adult cardiac interventions require significant ionizing radiation with potential health risks to both the patient and operator.

ASEF Grant Echo Can Dt Coronary Lesions Chest Pain Patients

The ASE Education and Research Foundation hosted a one-day event, Value-Based Healthcare: Summit 2014, Sept. 12 in Washington, D.C., which gathered thought leaders from across the healthcare...

October 3, 2014 — Esaote North America announced that its new MyLab Gamma ultrasound system has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) and is now available for...

Siemens Artis one

October 1, 2014 — St. Johns Hospital and Medical Center in Detroit recently became the first U.S. healthcare facility to install the Artis one angiography system from Siemens Healthcare. The Artis...

Backus Hospital, Hartford Hospital, The Hospital of Central Connecticut, MidState Medical Center, and Windham Hospital now gather and analyze dose data from all necessary modalities within their...

September 30, 2014 — The American College of Cardiology (ACC), along with eight partnering societies, released the first appropriate use criteria (AUC) for suspected heart disease in pediatric...

blood testing, nephrocheck

The U.S. Food and Drug Administration has allowed marketing of the NephroCheck test, a first-of-a-kind laboratory test to help determine if certain critically ill hospitalized patients are at risk...