ALT-001375K012887Amber Status
Medison America, Inc.
SA6000II DIAGNOSTIC ULTRASOUND SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001375FDA 510(k) · US (primary)
K012887Regulatory Registrations
🌐
US
FDA
ID: K012887
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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