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FDA 510(k) Applications Submitted by Connor Landgraf
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170874
03/24/2017
Eko Model E5 System (EME5), Eko DUO
Eko Devices, Inc.
K151319
05/18/2015
Eko Electronic Stethoscope System
Eko Devices, Inc.
K192004
07/26/2019
Eko Analysis Software
Eko Devices Inc
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