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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
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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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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