FDA Clears CorVista System With CAD Add-On
The FDA cleared the CorVista System with CAD Add-On to evaluate the presence of significant coronary artery disease as an aid in diagnosis.
The FDA cleared the CorVista System with CAD Add-On to evaluate the presence of significant coronary artery disease as an aid in diagnosis.
CorVista Health was granted Breakthrough Device Designation for a non-invasive diagnostic solution for those with pulmonary hypertension.
A new extravascular implantable cardioverter-defibrillator met safety and effectiveness goals for participants in a premarket clinical study.
The FDA cleared the CorVista System with CAD Add-On to evaluate the presence of significant coronary artery disease as an aid in diagnosis.
The Medtronic Heartware Ventricular Assist Device (HVAD) System may have a welding defect in the internal pump causing a malfunction.
Read MoreHigh-risk patients who need defibrillators to prevent cardiac arrest experience fewer complications with a device implanted under the skin.
Read MoreSpacelabs Healthcare demonstrated new diagnostic cardiology products at the American College of Cardiology’s annual event.
Read MoreKestra Medical Technologies’ ASSURE WCD system is effective at reducing false-positive shock alarms, according to clinical evaluation results.
Read MorePhysicians accessing GE Healthcare’s cardiac management system that integrates into the EMR, can interpret data in MUSE ECGs from patients.
Read MoreThese ablation catheters were approved to treat the growing prevalence of pediatric Atrioventricular Nodal Reentrant Tachycardia (AVNRT).
Read MoreRoyal Philips has unveiled a full-service, at-home, 12-lead electrocardiogram (ECG) solution for use in decentralized clinical trials.