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ALT-001221K001341Amber Status

Analogic Corp.

DR5000 DEDICATED CHEST X-RAY SYSTEM

All identifiers (2)
Aletia (canonical)ALT-001221
FDA 510(k) ยท US (primary)K001341

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K001341
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
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