Biotronik announced that the U.S. Food and Drug Administration (FDA) has approved its DX line of implantable cardioverter defibrillators (ICDs) that can deliver ultra-high energy on the first shock. Also included in the approval response from the...

Scientific confirmation has just been published in the American Journal of Cardiovascular Disease that atherosclerosis, the underlying process of heart attacks and strokes, is generally not caused by high cholesterol blood levels. It is r...

Minneapolis Heart Institute Foundation (MHIF) physicians are conducting a research study using the first transcatheter mitral valve replacement in the United States at Minneapolis Heart Institute at Abbott Northwestern Hospital.

Cardiovascular Systems Inc. announced that it has received U.S. Food and Drug Administration (FDA) clearance for the 4 French, 1.25 Solid Diamondback 360 Peripheral Orbital Atherectomy System (OAS) for the treatment of peripheral artery disea...

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Biotronik, DX, ICD, Inventra, Itrevia, FDA, ultra-high energy
Biotronik announced that the U.S. Food and Drug Administration (FDA) has approved its DX line of implantable cardioverter defibrillators (ICDs) that can...
Protek Duo, VV ECLS, CE mark, CardiacAssist, veno-venous cannula
CardiacAssist Inc. announced that it received a Class 3 CE-mark for its Protek Duo veno-venous cannula. The Protek Duo is licensed for use as a single...
atherosclerosis, vitamin C, heart disease, Dr. Rath Research Institute
Scientific confirmation has just been published in the American Journal of Cardiovascular Disease that atherosclerosis, the underlying process of heart attacks...
Icahn School of Medicine, Mount Sinai, Rush, tele-robotic ultrasound, telehealth
A new clinical trial is testing the feasibility and efficiency of a doctor in New York City remotely performing long-distance, tele-robotic ultrasound exams...
Biotronik, DX, ICD, Inventra, Itrevia, FDA, ultra-high energy
Biotronik announced that the U.S. Food and Drug Administration (FDA) has approved its DX line of implantable cardioverter defibrillators (
Cardiovascular Systems Inc. announced that it has received U.S. Food and Drug Administration (FDA) clearance for the 4 French, 1.25 Solid...
The HD Medical Inc. ViScope visual stethoscope product family provides dynamic auscultation — the ability to see what you hear. ViScope’s...
atherosclerosis, vitamin C, heart disease, Dr. Rath Research Institute
Scientific confirmation has just been published in the American Journal of Cardiovascular Disease that atherosclerosis, the underlying process of heart attacks...
Minneapolis Heart Institute Foundation, TMVR, Tendyne, FDA, first implant, U.S.
Minneapolis Heart Institute Foundation (MHIF) physicians are conducting a research study using the first transcatheter mitral valve replacement in the United...
ViScope
HD Medical Inc. demonstrated the new ViScope visual stethoscope product family at at HIMSS 15. These visual stethoscopes provide dynamic auscultation — the...
Boston Scientific, S-ICD, long-term data, TV-ICD, trial
The Journal of the American College of Cardiology published data confirming the long-term safety and efficacy of the Boston Scientific Corp. S-ICD System (...
U.S. healthcare reform is largely being driven through adoption of new information technology (IT...
4 days 19 hours ago
The biggest technology news coming out of the 2015 American College of Cardiology (ACC) annual...
4 weeks 4 days ago
It’s been no secret that the American healthcare system needed to change to survive economically...
10 weeks 4 days ago
Centricity, webinar, ZFV, ZFP, viewer, remote viewing system, enterprise
Healthcare organizations are demanding more capabilities for image viewers accessed by clinicians. Zero footprint (ZFP) viewers provide imaging tools from...
The webinar "State of the Art in MRI Pediatric Brain Perfusion Imaging" educates participants about the state of the art clinical and emerging translational...
This webinar discusses why contemporary adult cardiac interventions require significant ionizing radiation with potential health risks to both the patient and...

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January 5, 2015 — The first large-scale, multispecialty prospective clinical research trial to evaluate the use of...
January 27, 2015 — Health and Human Services Secretary Sylvia M. Burwell announced measurable goals and a timeline...
The U.S. Food and Drug Administration (FDA) has granted approval of Medtronic’s premarket approval application (PMA)...

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