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.
March 11, 2020
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