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Soliton Receives FDA Clearance Of Special 510(k) For Generation II Rapid Acoustic Pulse Device

Soliton, Inc., (NASDAQ:SOLY) ("Soliton" or the "Company"), a medical device company with a novel and proprietary platform technology licensed from The University of Texas on behalf of the MD Anderson

Benzinga · 03/11/2020 12:01

Soliton, Inc., (NASDAQ:SOLY) ("Soliton" or the "Company"), a medical device company with a novel and proprietary platform technology licensed from The University of Texas on behalf of the MD Anderson Cancer Center ("MD Anderson"), today announced U.S. Food and Drug Administration ("FDA") clearance of the Company's Special 510(k) Premarket Notification regarding its Generation II Rapid Acoustic Pulse ("RAP") device.