FDA grants 510(k) clearance for CardioInsight 3D mapping system
The FDA granted a 510(k) clearance for the CardioInsight noninvasive 3D mapping system, which provides 3D maps of the heart and is used to map irregular heart rhythms.
Medtronic announced the approval on Feb. 1.
Vivek Reddy, MD, of the Mount Sinai Hospital and Mount Sinai Health System in New York, was the first doctor to use the system in the U.S., according to Medtronic.
With the system, patients wear a 252-electrode sensor vest and have their atria or ventricles continuously and simultaneously mapped. The system collects electrocardiogram signals from the heart, while patients also undergo computed tomography scans.
Medtronic acquired CardioInsight Technologies for approximately $93 million in June 2015. CardioInsight’s ecVUE system, a noninvasive cardiac system that maps electrical disorders of the heart, received FDA 510(k) clearance in November 2014.