ALT-006764K213794Green Status
Eko Murmur Analysis Software (EMAS)
Eko Devices, Inc. · Manufacturer
All identifiers (2)
Aletia (canonical)
ALT-006764FDA 510(k) · US (primary)
K213794Overview
Accountability Tier
Tier 2
Regulatory Registrations
🌐
US
FDA
ID: K213794
510k
Lifecycle Signals
Last Automated Sync
Jun 2026
Last Clinical Review
Not reviewed
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