Olympus Surgical Video System Receives FDA 510(k) Clearance

Olympus, a medical and surgical products company, has announced that it has received FDA 510(k) clearance for its Articulating HD 3D Laparoscopic Surgical Video System, which is designed to improve accuracy by providing surgeons natural three-dimensional vision while performing laparoscopic procedures.

Sign up for our FREE GI E-Weekly for more coverage like this sent to your inbox!

The video system, which will be displayed at the Society of American Gastrointestinal and Endoscopy Surgeons 2013 Annual Meeting to be held April 17-20 in Baltimore, is fully compatible with the Olympus EVIS EXERA III endoscopy system.

More Articles on Gastroenterology:
American Cancer Society Awards Dr. Stephen Meltzer Research Grant
ResearchMoz Releases Endoscopy Market Outlook Report
8 Gastroenterology Devices Receive FDA 510(k) Clearance in March

Next Up in GI & Endoscopy

Olympus Surgical Video System Receives FDA 510(k) Clearance

Next Up in GI & Endoscopy

The studies shaping GI's future focus

GLP-1 drugs to lower colon cancer mortality: Study

CapsoVision seeks FDA nod for cancer screening capsule

How top hospitals are turning denials into ROI: 10 strategies

Next Up in GI & Endoscopy

The studies shaping GI's future focus

GLP-1 drugs to lower colon cancer mortality: Study

CapsoVision seeks FDA nod for cancer screening capsule

Join the 40,000+ ASC leaders who start their day with Becker's