ALT-001755K050840Amber Status
Bioview , Ltd.
MODIFICATION TO DUET SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001755FDA 510(k) · US (primary)
K050840Regulatory Registrations
🌐
US
FDA
ID: K050840
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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