FDA 510(k), K122550, ICS IMPULSE

FDA 510(k), K122550, ICS IMPULSE

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510(K) Number: K122550
Device Name: ICS IMPULSE
Manufacturer:
Device Classification Name: Nystagmograph
Regulation Number: 882.1460
Classification Product Code: GWN
Date Received: 08/21/2012
Decision Date: 02/01/2013
Regulation Medical Specialty: Neurology
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