ALT-001342K011624Amber Status
GE Medical Systems
EXPEDIO 500D R&F X-RAY SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001342FDA 510(k) · US (primary)
K011624Regulatory Registrations
🌐
US
FDA
ID: K011624
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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