ALT-001886K061755Amber Status
Esaote Europe B.V.
MYLAB15/20 NEW INDICATIONS ULTRASOUND SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001886FDA 510(k) ยท US (primary)
K061755Regulatory Registrations
๐
US
FDA
ID: K061755
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 Esaote Europe B.V., you can verify and update this listing.
