Eko Devices, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories2
Latest FDA decision2023-05-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K230111 | CORE 500 Digital Stethoscope | DQD | 2023-05-26 | View |
| 510(k) | K213794 | Eko Murmur Analysis Software (EMAS) | DQD | 2022-06-29 | View |
| 510(k) | K200776 | Eko CORE | DQD | 2020-04-06 | View |
| 510(k) | K192004 | Eko Analysis Software | MWI | 2020-01-15 | View |
| 510(k) | K170874 | Eko Model E5 System (EME5), Eko DUO | DQD | 2017-05-19 | View |
No matching devices.
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