ALT-001900K062247Amber Status
Philips Ultrasound, Inc.
HD11 DIAGNOSTIC ULTRASOUND SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001900FDA 510(k) ยท US (primary)
K062247Regulatory Registrations
๐
US
FDA
ID: K062247
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 Philips Ultrasound, Inc., you can verify and update this listing.
