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FDA 510(k) Applications Submitted by BRAINSCOPE COMPANY, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190815
03/29/2019
BrainScope TBI
BrainScope Company, Inc.
K082886
09/30/2008
ZOOM-100DC
BRAINSCOPE COMPANY, INC.
K143643
12/22/2014
Brainscope Ahead 200
BRAINSCOPE COMPANY, INC.
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