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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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