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FDA 510(k) Application Details - K112107
Device Classification Name
Electroencephalograph
More FDA Info for this Device
510(K) Number
K112107
Device Name
Electroencephalograph
Applicant
NEUROVIRTUAL USA, INC.
2315 NW 107TH AVE
SUITE #1M27
DORAL, FL 33172 US
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Contact
EDUARDO FARIA
Other 510(k) Applications for this Contact
Regulation Number
882.1400
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Classification Product Code
GWQ
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More FDA Info for this Product Code
Date Received
07/22/2011
Decision Date
10/28/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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