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EDAP Receives U.S. FDA 510(k) Approval for Sonolith I-Sys

Novel, Innovative and Robotized Next-Generation Lithotripsy Device to Enter U.S. Market LYON, France, Aug. 19, 2009 –(HSMN NewsFeed) — EDAP TMS SA (Nasdaq:EDAP ), the global leader in therapeutic ultrasound, announced today that the U.S. Food and Drug…
Devices, Urology, FDA
EDAP TMS, Sonolith I-Sys, lithotripsy, high-intensity focused ultrasound

EDAP Receives U.S. FDA 510(k) Approval for Sonolith I-Sys

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