BRIEF-Brainsway Says It Received U.S. FDA 510(K) Clearance For Its New Stimulator

May 6 (Reuters) – Brainsway Ltd:

* RECEIVED U.S. FDA 510(K) CLEARANCE FOR ITS NEW STIMULATOR

* NEW STIMULATOR TO BE INTEGRATED INTO COS DEEP TRANSCRANIAL MAGNETIC STIMULATION SYSTEM FOR TREATMENT OF MAJOR DEPRESSIVE DISORDER (MDD) Source text for Eikon: Further company coverage:



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