Philips Alerts Customers to Missed Cardiac Telemetry Notifications
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
Restore Medical's ContraBand device received FDA Breakthrough Device Designation for treating heart failure with reduced ejection fraction.
Ultromics' EchoGo Heart Failure, an AI solution for echocardiography to help diagnosis heart failure, received FDA clearance.
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
Medtronic announced its LINQ II Insertable Cardiac Monitor system received 510(k) clearance by the U.S. FDA for use in pediatric patients.
Read MoreThe U.S. FDA is alerting healthcare providers about potential malfunctions with MitraClip Clip Delivery Systems manufactured by Abbott.
Read MorePrepMD RMS, a cardiac clinical solutions company, acquired the intellectual property of a health company specializing in remote monitoring.
Read MoreA new extravascular implantable cardioverter-defibrillator met safety and effectiveness goals for participants in a premarket clinical study.
Read MoreUsing a suspended nanowire, researchers created a tiny sensor that measures electrical and mechanical cellular responses in cardiac tissue.
Read MoreBiotronik will pay $12.95 million to resolve allegations of violating the False Claims Act via the submission of false claims.
Read MoreThe U.S. FDA has cleared Eko's Murmur Analysis Software for detecting and characterizing murmurs found in adults and pediatric patients.