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FDA 510(k) Applications Submitted by electroCore, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180538
02/28/2018
gammaCore Sapphire
electroCore, LLC
K171306
05/03/2017
gammaCore-S
electroCore, LLC
DEN150048
10/16/2015
gammaCore Non-invasive Vagus Nerve Stimulator
electroCore, LLC
K173442
11/06/2017
gammaCore-S
electroCore, LLC
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