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FDA 510(k)

MindMotion(TM) GO

K-Number: K173931 · 2018-05-17

ApplicantMindmaze SA
Decision Date2018-05-17
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MindMotion(TM) GO is a medical device manufactured by Mindmaze SA. It received FDA 510(k) clearance on 2018-05-17 under approval number K173931. The device is classified under product code LXJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MindMotion(TM) GO?

MindMotion(TM) GO is a medical device that received FDA 510(k) clearance on 2018-05-17. It is manufactured by Mindmaze SA. The 510(k) number is K173931.

When was MindMotion(TM) GO approved by the FDA?

MindMotion(TM) GO received FDA 510(k) clearance on 2018-05-17, under approval number K173931.

What company makes MindMotion(TM) GO?

MindMotion(TM) GO is manufactured by Mindmaze SA.

What is the FDA product code for MindMotion(TM) GO?

The FDA product code for MindMotion(TM) GO is LXJ.

Other Devices by Mindmaze SA

K162748MindMotionPRO

Related Devices (Code: LXJ)

K151955YuGo SystemBiogaming , Ltd. K162748MindMotionPROMindmaze SA K163245Virtual Occupational Therapy Application (VOTA)Barron Associates, Inc. K171547Qualisys Clinical SystemQualisys AB K172882UINCARE HOMEUincare Corp. K192474VERAReflexion Health, Inc.

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.

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