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01/27/2016SonarMed Receives Clearance for its one of a kind Pediatric Airway Monitor
 

SonarMed receives FDA clearance for real-time monitoring device for endotracheal tubes in pediatric patients

Carmel, Indiana, February 1, 2016-----SonarMed announced today that they received FDA 510(k) clearance for their AirWave Monitoring System for neonatal (newborn) and pediatric patients, a new device that provides real-time monitoring of the endotracheal tube, a tube inserted into the windpipe to aid in breathing. The SonarMed AirWave system pioneered the use of acoustic reflectometry to continuously monitor the endotracheal tube for movement and obstruction. 

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