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FDA 510(k), K150641, MagVita TMS Therapy System
FDA 510(k), K150641, MagVita TMS Therapy System
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510(K) Number: K150641
Device Name: MagVita TMS Therapy System
Manufacturer: TONICA ELEKTRONIK A/S
Device Classification Name: transcranial magnetic stimulator
Regulation Number: 882.5805
Classification Product Code: OBP
Date Received: 03/11/2015
Decision Date: 07/31/2015
Regulation Medical Specialty: Neurology
Device Name: MagVita TMS Therapy System
Manufacturer: TONICA ELEKTRONIK A/S
Device Classification Name: transcranial magnetic stimulator
Regulation Number: 882.5805
Classification Product Code: OBP
Date Received: 03/11/2015
Decision Date: 07/31/2015
Regulation Medical Specialty: Neurology
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- 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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