FDA 510(k), K182768, TMS-Cobot TS MV

FDA 510(k), K182768, TMS-Cobot TS MV

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510(K) Number: K182768
Device Name: TMS-Cobot TS MV
Manufacturer: Axilum Robotics
Device Classification Name: electromechanical arm for a transcranial magnetic stimulation system
Regulation Number: 882.5805
Classification Product Code: QFF
Date Received: 09/28/2018
Decision Date: 02/17/2019
Regulation Medical Specialty: Neurology

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