FDA 510(k) Applications Submitted by Eko Health, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K233409 | 10/06/2023 | Eko Low Ejection Fraction Tool (ELEFT) | Eko Health, Inc. |
| K233609 | 11/13/2023 | CORE 500 Digital Stethoscope | Eko Health, Inc. |
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