Varian Medical Systems has obtained FDA 510(k) clearance to market the Nexus DR, a high-resolution x-ray system utilizing a digital radiography detector. A single common imaging platform for general radiographic procedures (excluding fluoroscopy, angiography, and mammography), the Nexus DR can replace conventional film techniques or existing digital systems in multipurpose or dedicated applications.
Read More
Carestream has secured FDA 510(k) clearance for its OnSight 3D Extremity System, which is available for order in the United States. The system, which will be demonstrated at the American Society for Surgery of the Hand conference that runs from September 29 to October 1 in Austin, Texas, leverages cone-beam CT technology to secure weight-bearing and other types of extremity exams.
Read More
In October, during “Breast Cancer Awareness Month,” many women will be reminded of the importance of an annual mammogram. This potentially life-saving test has long been an important tool for preventing breast cancer deaths in women 40 and older of average risk. In this article, 24×7 explores all the imaging modalities related to breast imaging.
Read More
The FDA has notified healthcare and industry professionals about the “serious clinical consequences” that can arise from using programmable syringe pumps to infuse therapies at low rates. To help protect particularly vulnerable patients from potential treatment delays or over- or under-infusion, the agency has requested that manufacturers include new information and warnings in their instructions for use.
Read More
While “smart” infusion pumps are designed with patient safety in mind, it’s up to clinicians and support staff, such as HTM professionals, to ensure they perform as manufacturers advertise. Seasoned 24×7 writer Chris Hayhurst took an in-depth look at the smart pump revolution in October’s cover story. Don’t miss out.
Read More