The CorPath 200 cath lab robotic system is designed for more precise movements and less radiation exposure to physicians during PCI.

Feature | July 25, 2012

July 25, 2012 — Corindus Vascular Robotics today announced U.S. Food and Drug Administration (FDA) 510(k) clearance...

Feature | July 24, 2012 | Brian Duncan, St. Mary’s Healthcare System

St. Mary’s Healthcare System is a 199-bed hospital in Athens, Ga., and has been a trusted presence in the community...

Videos | Vena Cava Filters | July 24, 2012

This video, provided by Crux Biomedical, demonstrates the implantation of the FDA-cleared Crux VCF inferior vena...

News | July 24, 2012

July 24, 2012 — Use of the retrograde approach to revascularizing coronary...

Technology | July 24, 2012

July 24, 2012 — The importance of utilizing...

Technology | July 24, 2012

July 24, 2012 — GE Healthcare announced U.S. Food and Drug Administration (FDA) 510(k) clearance of its new cardiac...

News | July 23, 2012

July 23, 2012 — Biotronik announced that the first CRT-D patient has been enrolled in the Biotronik EuroEco Trial —...

News | July 23, 2012

July 23, 2012 — The IT and medical technology company Sectra has acquired the product rights for Intulo, a system...

Technology | July 23, 2012

July 23, 2012 — Siemens Healthcare expands its ultrasound portfolio with the portable Acuson P300...

News | July 23, 2012

July 23, 2012 — Medtronic Inc. announced the first patient enrollment in a global, multicenter, randomized clinical...

Feature | July 20, 2012

July 20, 2012 — Ticagrelor (Brilinta), a blood-thinning drug approved by the U.S. Food and Drug Administration (FDA...

News | July 20, 2012

July 20, 2012 — The online clinical drug resource Drugs.com released first quarter 2012 U.S. prescription sales data...

News | July 20, 2012

July 20, 2012 — The ability to see inside the arteries of vascular disease patients in high resolution before and...

Technology | July 20, 2012

July 20, 2012 — Crux Biomedical announced it has received U.S. Food and Drug Administration (FDA) clearance for its...

News | July 20, 2012

July 20, 2012 — Acusphere Inc. announced that it had completed the marketing authorization application (MAA) dossier...

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