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Medigus Receives FDA 510(k) Clearance for SRS Endoscopic System

Written by  Rob Kurtz | June 04, 2012
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Medigus has announced it has received FDA 510(k) marketing clearance for its SRS endoscopic system, according to a news release.


The device is intended for minimally-invasive endoluminal treatment of GERD.


The endoscope is inserted into the esophagus through the mouth and does not entail incisions into the abdominal cavity. The endoscope features a miniature video camera, ultrasonic sights and a stapling device that enables the physician to perform partial fundoplication.


Medigus already possesses a CE mark for the SRS system.


Medigus is headquartered in Omer, Israel.


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