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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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