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FDA 510(k) Applications Submitted by HEATHER BELL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K201114
04/27/2020
Bidop 7
Koven Technology, Inc.
K143332
11/20/2014
Fast Sphyg by Koven
KOVEN TECHNOLOGY, INC.
K153762
12/30/2015
Smartdop XT6
KOVEN TECHNOLOGY, INC.
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