FDA 510(k), K131383, X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE

FDA 510(k), K131383, X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE

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510(K) Number: K131383
Device Name: X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE
Manufacturer: ADVANCED BRAIN MONITORING INC.
Device Classification Name: full-montage standard electroencephalograph
Regulation Number: 882.1400
Classification Product Code: GWQ
Date Received: 05/14/2013
Decision Date: 11/27/2013
Regulation Medical Specialty: Neurology

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