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Eko Devices, Inc.

6 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
CORE 500 Digital Stethoscope (K230111)Eko Devices, Inc.2023-05-26
Eko Murmur Analysis Software (EMAS) (K213794)Eko Devices, Inc.2022-06-29
Eko CORE (K200776)Eko Devices, Inc.2020-04-06
Eko Analysis Software (K192004)Eko Devices, Inc.2020-01-15
Eko Model E5 System (EME5), Eko DUO (K170874)Eko Devices, Inc.2017-05-19
Eko Electronic Stethoscope System (K151319)Eko Devices, Inc.2015-08-28

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