ALT-001221K001341Amber Status
Analogic Corp.
DR5000 DEDICATED CHEST X-RAY SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001221FDA 510(k) ยท US (primary)
K001341Regulatory Registrations
๐
US
FDA
ID: K001341
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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