FDA 510(k)

MindMotion(TM) GO

K-Number: K173931 · 2018-05-17

Decision Date2018-05-17

Product CodeLXJ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MindMotion(TM) GO is the device name listed in this FDA 510(k) record. The listed applicant is Mindmaze SA. It received FDA 510(k) clearance on 2018-05-17 under 510(k) 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. The listed applicant is Mindmaze SA. The 510(k) number is K173931.

When did MindMotion(TM) GO receive FDA 510(k) clearance?

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

Who is the listed applicant for MindMotion(TM) GO?

The FDA 510(k) record lists Mindmaze SA as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Mindmaze SA as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K162748MindMotionPRO

Related Devices (Code: LXJ)

K192474VERAReflexion Health, Inc.K182333VeraReflexion Health, Inc.K180880DARI HealthScientific Analytics, Inc.K171547Qualisys Clinical SystemQualisys AB K172882UINCARE HOMEUincare Corp.K162748MindMotionPROMindmaze SA

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.