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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