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FDA grants breakthrough status to Ceribell’s AI EEG tool for faster in-hospital stroke detection.
Ceribell has received FDA Breakthrough Device Designation for an AI-powered EEG system that detects large vessel occlusion strokes in hospitalized patients, aiming to reduce delays in diagnosis and treatment.
The technology uses existing hardware and an advanced algorithm to analyze brainwave signals, addressing a critical gap in in-hospital stroke care where early detection is often limited.
The FDA’s designation accelerates development and review, building on prior clearances for neonatal seizure and delirium monitoring.
In-hospital strokes, which account for up to 17% of annual U.S. cases, face higher mortality and worse outcomes due to delayed intervention.
The system supports continuous bedside monitoring and could improve recovery rates.
La FDA otorga el estatus de avance a la herramienta EEG AI de Ceribell para una detección más rápida de accidentes cerebrovasculares en el hospital.