FDA 510(k) Applications Submitted by Richard Waite

FDA 510(k) Number Submission Date Device Name Applicant
K200276 02/04/2020 SPEAC System Brain Sentinel, Inc.
K140805 04/01/2014 ITCLAMP 50 INNOVATIVE TRAUMA CARE INC
K161704 06/20/2016 Phasor Drill BIOTEX, INC.
K182180 08/13/2018 SPEAC System Brain Sentinel, Inc.
K132651 08/26/2013 ITCLAMP 50 INNOVATIVE TRAUMA CARE INC
K123551 11/19/2012 ITCLAMP 50 INNOVATIVE TRAUMA CARE INC


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