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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