ALT-007191K131044Green Status
SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION
DIACOUSTIC MEDICAL DEVICES (PTY) LTD. · Manufacturer
All identifiers (2)
Aletia (canonical)
ALT-007191FDA 510(k) · US (primary)
K131044Overview
Accountability Tier
Tier 2
Regulatory Registrations
🌐
US
FDA
ID: K131044
510k
Lifecycle Signals
Last Automated Sync
Jun 2026
Last Clinical Review
Not reviewed
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