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FDA 510(k)

MindMotionPRO

K-Number: K162748 · 2017-04-24

ApplicantMindmaze SA
Decision Date2017-04-24
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MindMotionPRO is a medical device manufactured by Mindmaze SA. It received FDA 510(k) clearance on 2017-04-24 under approval number K162748. 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 MindMotionPRO?

MindMotionPRO is a medical device that received FDA 510(k) clearance on 2017-04-24. It is manufactured by Mindmaze SA. The 510(k) number is K162748.

When was MindMotionPRO approved by the FDA?

MindMotionPRO received FDA 510(k) clearance on 2017-04-24, under approval number K162748.

What company makes MindMotionPRO?

MindMotionPRO is manufactured by Mindmaze SA.

What is the FDA product code for MindMotionPRO?

The FDA product code for MindMotionPRO is LXJ.

Other Devices by Mindmaze SA

K173931MindMotion(TM) GO

Related Devices (Code: LXJ)

K151955YuGo SystemBiogaming , Ltd. K163245Virtual Occupational Therapy Application (VOTA)Barron Associates, Inc. K171547Qualisys Clinical SystemQualisys AB K173931MindMotion(TM) GOMindmaze SA 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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