ALT-001384K013150Amber Status
Ultraguide , Ltd.
MR-GUIDE 2000
All identifiers (2)
Aletia (canonical)
ALT-001384FDA 510(k) · US (primary)
K013150Regulatory Registrations
🌐
US
FDA
ID: K013150
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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