Natus Medical Submits FDA 510(k) for Point-of-Care EEG Device
Natus Medical submitted an FDA 510(k) notification for its point-of-care EEG device, designed to identify seizures in acute care settings.
Natus Medical submitted an FDA 510(k) notification for its point-of-care EEG device, designed to identify seizures in acute care settings.
Siemens Healthineers has received U.S. FDA clearance for the AI-powered Acuson Origin cardiovascular ultrasound system and the AcuNav Lumos 4D ICE catheter, both designed to improve cardiac diagnostics and patient care.
Clarius Mobile Health has received U.S. FDA clearance for its OB AI tool, which uses deep learning to provide accurate fetal measurements.
Natus Medical submitted an FDA 510(k) notification for its point-of-care EEG device, designed to identify seizures in acute care settings.
Leveraging advanced technologies like predictive work systems, RTLS, and AI helps health systems proactively prevent equipment failures, one industry expert says.
Read MoreRoyal Philips and Nicklaus Children’s Health System began a 10-year collaboration on pediatric care with new MR and ultrasound technology.
Read MoreEpitel announced FDA clearance for two technologies: REMI Remote EEG Monitoring System for home use and REMI Vigilenz AI for Event Detection.
Read MoreGE HealthCare has launched the Voluson Signature 20 and 18 ultrasound systems, integrating AI, advanced tools, and ergonomic design.
Read MoreGE HealthCare launched Caption AI software for rapid cardiac assessments at the point of care on Vscan Air SL.Â
Read MoreAn unnamed health system has partnered with Healthcare Triangle to utilize its cloud-based AI and machine learning solution for patient data.Â
Read MoreDiagnaMed Holdings, announced that Drexel University will be a test launch site of CERVAI, a consumer brain health and wellness AI solution.Â