The U.S. Food and Drug Administration (FDA) cleared Carestream Health’s Vue Motion image viewer for clinical viewing and reading of medical X-ray exams using iPhone 4s, iPad 2, Galaxy Note and Galaxy S III mobile devices. Â
HealthMed Holdings completed validation on a blood test that aims to identify individuals who are at risk of a heart attack and may be missed by conventional tests.Â
These individuals have no symptoms and frequently have normal standard blood cholesterol profiles, but are at significant risk of having a heart attack in the near term. The group is actively commercializing the test.
Carestream is sponsoring an executive panel discussion at the HIMSS 2014 meeting, Feb. 25, from 3:30 to 4:30 p.m. in Room 202C at the Orlando Convention Center. The title is “Executive Perspective: How to Achieve Efficient Enterprise Data Management” and the session is open to all HIMSS attendees. Jennifer Horowitz, Senior Director of Research for HIMSS Analytics, will be the moderator.
A team of interventional cardiologists and cardiovascular surgeons at The University of Texas Health Science Center at Houston (UTHealth) and Memorial Hermann Heart & Vascular Institute-Texas Medical Center performed Texas’ first transcatheter aortic valve replacement (TAVR) under conscious sedation using the Edwards Sapien valve.
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The U.S. Food and Drug Administration (FDA) granted AliveCor Inc. over-the-counter (OTC) clearance for the AliveCor Heart Monitor, a single-channel ECG (electrocardiogram) recorder, previously available by prescription only. The device is available for pre-order purchase with shipments beginning in March.
Wolters Kluwer Health, a global provider of information for healthcare professionals and students, will make available at HIMSS13 Annual Conference & Exhibition the UpToDate. Anywhere. The product enables healthcare enterprises to improve patient care by equipping clinicians with anytime/anywhere access to comprehensive, evidence-based, clinical decision support through the UpToDate mobile app.