ALT-001910K062623Amber Status
Siemens Medical Solutions USA, Inc.
AXIOM LUMINOS DRF
All identifiers (2)
Aletia (canonical)
ALT-001910FDA 510(k) · US (primary)
K062623Regulatory Registrations
🌐
US
FDA
ID: K062623
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
Some fields are incomplete or unverified. If you represent Siemens Medical Solutions USA, Inc., you can verify and update this listing.