ALT-001351K012080Amber Status
Aloka Co., Ltd.
SSD-5000 DIAGNOSTIC ULTRASOUND SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001351FDA 510(k) · US (primary)
K012080Regulatory Registrations
🌐
US
FDA
ID: K012080
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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