ALT-001770K051534Amber Status
Et Medical Devices Spa
CARDIOLINE AR 600, AR 1200, AR 2100
All identifiers (2)
Aletia (canonical)
ALT-001770FDA 510(k) ยท US (primary)
K051534Regulatory Registrations
๐
US
FDA
ID: K051534
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 Et Medical Devices Spa, you can verify and update this listing.
