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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