1. Device For Detecting Pre-Cancerous Barrett's Esophagus Receives FDA Clearance

    Device For Detecting Pre-Cancerous Barrett's Esophagus Receives FDA Clearance

    The test involves a swallowable balloon device that samples the esophagus and a DNA assay that detects Barrett’s esophagus and esophageal cancers. In a major step to bringing this technology forward to patients, the balloon device has just received 510K clearance from the U.S. Food and Drug Administration (FDA) for clinical use. The device is being manufactured by Lucid Diagnostics and marketed under the tradename EsoCheck.

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