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

Medigus has announced it has received FDA 510(k) marketing clearance for its SRS endoscopic system, according to a news release.

Advertisement

 

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.

 

Related Articles on FDA Clearances:

Boston Scientific Receives FDA Clearance for Expanded Use Indication for Wire-Guided Balloon Dilator

EndyMed Medical Receives FDA Clearance for Dermatologic Procedure Device

Teleflex Receives FDA Clearance for Epidural Catheter

Advertisement

Next Up in Uncategorized

Advertisement