Eko Health, Inc.

Eko Health, Inc. holds 4 FDA 510(k) medical device clearances, first cleared 2024, most recent 2026.

Top product codes for Eko Health, Inc.

DQD — Cardiovascular3 devices
QYE — Cardiovascular1 device

Recent clearances by Eko Health, Inc.

K261694 — CORE 300 Digital StethoscopeCode DQD·2026-07-23
K251494 — Eko Foundation Analysis Software with Transformers (EFAST)Code DQD·2025-08-12
K233409 — Eko Low Ejection Fraction Tool (ELEFT)Code QYE·2024-03-28
K233609 — CORE 500 Digital StethoscopeCode DQD·2024-03-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.