FDA 510(k), K173931, MindMotion(TM) GO

FDA 510(k), K173931, MindMotion(TM) GO

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510(K) Number: K173931
Device Name: MindMotion(TM) GO
Manufacturer: Sylvian Bourriquet
Device Classification Name: Interactive Rehabilitation Exercise Devices
Regulation Number: LXJ
Classification Product Code: KXA
Date Received: 12/26/2017
Decision Date: 05/17/2018
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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