FDA 510(k)

MagVita TMS Therapy - w/MagPro R20

K-Number: K170114 · 2017-05-01

Decision Date2017-05-01

Product CodeOBP

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MagVita TMS Therapy - w/MagPro R20 is a medical device manufactured by Tonica Elektronik A/S. It received FDA 510(k) clearance on 2017-05-01 under approval number K170114. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MagVita TMS Therapy - w/MagPro R20?

MagVita TMS Therapy - w/MagPro R20 is a medical device that received FDA 510(k) clearance on 2017-05-01. It is manufactured by Tonica Elektronik A/S. The 510(k) number is K170114.

When was MagVita TMS Therapy - w/MagPro R20 approved by the FDA?

MagVita TMS Therapy - w/MagPro R20 received FDA 510(k) clearance on 2017-05-01, under approval number K170114.

What company makes MagVita TMS Therapy - w/MagPro R20?

MagVita TMS Therapy - w/MagPro R20 is manufactured by Tonica Elektronik A/S.

What is the FDA product code for MagVita TMS Therapy - w/MagPro R20?

The FDA product code for MagVita TMS Therapy - w/MagPro R20 is OBP.

Other Devices by Tonica Elektronik A/S

K160280MagPro R20 K172667MagVita TMS Therapy w/MagPro R20 K171967MagVita TMS Therapy System K171481MagVita TMS Therapy System K162873MEP Monitor K173620Mag Vita TMS Therapy System w/Theta Burst Stimulation

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Related Devices (Code: OBP)

K160309Neurosoft TMSTeleemg, LLC K161519NeuroStar TMS Therapy SystemNeuronetics, Inc. K160703NeuroStar TMS Therapy SystemNeuronetics, Inc. K173441Neurosoft TMS (also CloudTMS)Teleemg, LLC K171902Nexstim Navigated Brain Therapy (NBT) System 2Nexstim Plc K172667MagVita TMS Therapy w/MagPro R20Tonica Elektronik A/S

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.