Medical Device Network on MSN1d
FDA grants expanded 510(k) clearance for Epitel’s wireless EEG system
This is the fifth 510(k) clearance for the company’s REMI portfolio, with the first clearance obtained in March 2021.
Morningstar2d
Epitel’s REMI Wireless Wearable EEG System Receives Expanded FDA Clearance for Patients as Young as One Year Old
Traditional EEG monitoring often involves cumbersome ... where near real-time and/or remote EEG is warranted and in ambulatory settings where remote EEG is warranted. REMI System uses single ...
Hosted on MSN28d
Brain waves measured during sleep predict cognitive impairment years before symptoms appear, study finds
More information: Shahab Haghayegh et al. Predicting future risk of developing cognitive impairment using ambulatory sleep EEG: Integrating Univariate Analysis and Multivariate Information Theory ...
Medscape1mon
Pseudoseizures: Evaluation and Treatment
When EEG activation fails to clarify the diagnosis, a patient can be fitted with an ambulatory EEG recording device that is worn as he or she conducts daily life activities. The patient either ...
Medscape17d
Outpatient seizure identification: results of 502 patients using computer-assisted ambulatory EEG.
The goal of this study was to assess the frequency of unreported seizures recorded during routine outpatient ambulatory EEG recording. The authors reviewed 552 records from 502 patients who ...
Baylor College of Medicine4y
Clinical Neurophysiology Fellowship
The program includes training in outpatient and inpatient EEG (adult and pediatric) including continuous video EEG monitoring, ambulatory EEG, quantitative EEG, evoked potentials, polysomnography, ...
Epitel’s REMI Wireless Wearable EEG System Receives Expanded FDA Clearance for Patients as Young as One Year Old
Revolutionary brain health monitoring system REMI is now cleared for EEG use in infants and children as young as one year old.