FDA 510(k), K131434, VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
FDA 510(k), K131434, VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Device Name: VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Manufacturer:
Device Classification Name: Endoscope, Neurological
Regulation Number: 882.1480
Classification Product Code: GWG
Date Received: 05/17/2013
Decision Date: 07/16/2013
Regulation Medical Specialty: Neurology
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