FDA 510(k), K041263, NEUROGUIDE ANALYSIS SYSTEM

FDA 510(k), K041263, NEUROGUIDE ANALYSIS SYSTEM

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510(K) Number: K041263
Device Name: NEUROGUIDE ANALYSIS SYSTEM
Manufacturer:
Device Classification Name: Normalizing Quantitative Electroencephalograph Software
Regulation Number: 882.1400
Classification Product Code: OLU
Date Received: 05/11/2004
Decision Date: 08/03/2004
Regulation Medical Specialty: Neurology
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