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Corindus Vascular Robotics, a leading developer of precision vascular robotics, today announced FDA 510(k) clearance has been granted for the CorPath 200 System to be used in percutaneous coronary interventions (PCI). The technology is now approved in the United States to assist interventional cardiologists in performing PCI, a procedure to restore blood flow to blocked arteries in patients with coronary artery disease (CAD).
“We are pleased to have received clearance from the FDA for the world’s first system designed for robotic-assisted PCI procedures,” said David M. Handler, President and CEO of Corindus Vascular Robotics. “This is an important milestone for interventional cardiology as we take the next step in transforming the way these procedures are performed in the future. The CorPath System offers hospitals the opportunity to bring robotic-assisted technology benefits to their coronary patients and their physicians.”
To view Multimedia News Release, go to http://www.multivu.com/mnr/57343-corindus-vascular-robotics-wins-fda-510k-clearance-for-corpath-200-system
Hot Spring® Spas, the world’s leading spa brand, congratulated Don Benecke, of Osage Beach, Missouri, as the winner in the June Hot Spring Salt Water Hot Tub Giveway. Benecke won the Hot Spring spa model of his choice – complete with the revolutionary ACE® Salt Water Sanitizing System, the proprietary CoverCradle® cover lifter, and a matching Everwood® step. To enter the Giveaway, contestants were encouraged to “Like” the Hot Spring Spas Facebook page and then watch a fun, animated video to find out why ‘diamonds are a hot tub’s best friend’. To increase their chances of winning, contestants were encouraged to share the video with friends.
To view Multimedia News Release, go to http://www.multivu.com/mnr/57463-hot-spring-spas-awards-salt-water-hot-tub-to-long-time-fan
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The Alfred Mann Foundation (AMF) today announced the first subject, a U.S. Marine, SSgt James Sides, as a recipient of its highly anticipated IMES System (implantable myoelectric sensor) – an experimental system that holds the promise of being the first minimally invasive, intuitive, multi-channel control system for prosthetics intended for long term use. The IMES System is currently being studied under the Investigational Device Exemption (IDE) regulations of the U.S. Food and Drug Administration (FDA). AMF’s ongoing trial with injured veterans at the Walter Reed National Medical Military Center anticipates subjects intuitively operating three different prosthetic movements simultaneously: opening and closing the hand, rotating the wrist, and moving the thumb. Combining these three movements enables several grasps that are invaluable for performing everyday tasks.
To view the Multimedia News Release, go to http://www.multivu.com/mnr/65112-alfred-mann-foundation-u-s-marine-subject-fda-study-for-imes-system
This week Hill-Rom (NYSE: HRC) is featuring the Progressa® bed system, the next generation of intensive care unit (ICU) bed systems, at the American Organization of Nurse Executives (AONE) annual meeting in Orlando, Fla. The Progressa bed system is a therapeutic system designed to treat and prevent complications of immobility. It features a state-of-the-art design that supports treatment goals and was engineered to help address patient migration via its StayInPlace™ technology.
To view the Multimedia News Release, go to http://www.multivu.com/mnr/66137-hill-rom-new-progressa-bed-system
The main benefits of this revolutionary filling system are high output & low manning, relatively short investment payback time and health/environment & safety advantages. The system also opens up possibilities to centralize filling operations with integrated system suppliers through cooperation which ensures smooth start-up and simpler support.
The two companies, Erkomat Oy and Thrace Polybulk, have in close cooperation become the leading global supplier of fully automatic filling systems for FIBCs (also called big-bags or bulk bags).
To view the Multimedia News Release, go to http://www.multivu.com/mnr/7140056-erkojet-big-bag-packing-system
Edwards Lifesciences Corporation (NYSE: EW), the global leader in the science of heart valves and hemodynamic monitoring, today announced it has received U.S. Food and Drug Administration (FDA) clearance for the ClearSight system.
The ClearSight system is a noninvasive monitor that provides clinicians access to valuable blood volume and blood flow information for patients at moderate or high risk of post-surgical complications, in whom invasive monitoring would not be used.
To view the Multimedia News Release, go to http://www.multivu.com/players/English/7256451-edwards-fda-clearance-for-noninvasive-hemodynamic-monitoring-system/
