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FDA 510(k) K142494, ViMove, by Dorsavi, Ltd.

FDA 510(k) K142494, ViMove, by Dorsavi, Ltd.

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510(K) Number: K142494
Device Name: ViMove
Manufacturer: Dorsavi, Ltd.
Device Classification Name: electromyograph, diagnostic
Regulation Number: 890.1375
Classification Product Code: IKN
Date Received: 09/05/2014
Decision Date: 05/28/2015
Regulation Medical Specialty: Physical Medicine
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