FDA 510(k) Application Details - K141865

Device Classification Name Recorder, Attention Task Performance

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510(K) Number K141865
Device Name Recorder, Attention Task Performance
Applicant ANTHROTRONIX, INC
8737 COLESVILLE ROAD
SUITE L-203
SILVER SPRING, MD 20910 US
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Contact CORINA E LATHAN, PHD, PE
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Regulation Number 000.0000

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Classification Product Code LQD
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Date Received 07/10/2014
Decision Date 10/15/2014
Decision SESE - SUBST EQUIV
Classification Advisory Committee -
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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