FDA 510(k), K122288, BRAINSWAY DEEP TMS SYSTEM

FDA 510(k), K122288, BRAINSWAY DEEP TMS SYSTEM

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510(K) Number: K122288
Device Name: BRAINSWAY DEEP TMS SYSTEM
Manufacturer: BRAINSWAY, LTD
Device Classification Name: transcranial magnetic stimulator
Regulation Number: 882.5805
Classification Product Code: OBP
Date Received: 07/30/2012
Decision Date: 01/07/2013
Regulation Medical Specialty: Neurology
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