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FDA 510(k), K173931, MindMotion(TM) GO
FDA 510(k), K173931, MindMotion(TM) GO
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$149.00 USD
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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: 12/26/2017
Date Received: 05/17/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Device Name: MindMotion(TM) GO
Manufacturer: Sylvian Bourriquet
Device Classification Name: Interactive Rehabilitation Exercise Devices
Regulation Number: LXJ
Classification Product Code: 12/26/2017
Date Received: 05/17/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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