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FDA 510(k), K173620, Mag Vita TMS Therapy System w/Theta Burst Stimulation
FDA 510(k), K173620, Mag Vita TMS Therapy System w/Theta Burst Stimulation
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510(K) Number: K173620
Device Name: Mag Vita TMS Therapy System w/Theta Burst Stimulation
Manufacturer: Tonica Elektronik A/S
Device Classification Name: Transcranial Magnetic Stimulator
Regulation Number: 882.5805
Classification Product Code: OBP
Date Received: 11/22/2017
Decision Date: 08/14/2018
Regulation Medical Specialty: Neurology
Device Name: Mag Vita TMS Therapy System w/Theta Burst Stimulation
Manufacturer: Tonica Elektronik A/S
Device Classification Name: Transcranial Magnetic Stimulator
Regulation Number: 882.5805
Classification Product Code: OBP
Date Received: 11/22/2017
Decision Date: 08/14/2018
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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