ALT-006651K223771Green Status
Lumify Diagnostic Ultrasound System
Philips Ultrasound · Manufacturer
All identifiers (4)
Aletia (canonical)
ALT-006651FDA 510(k) · US (primary)
K223771FDA 510(k) · US
K252557FDA 510(k) · US
K232500Overview
Accountability Tier
Tier 2
Regulatory Registrations
🌐
US
FDA
ID: K223771
510k
Lifecycle Signals
Last Automated Sync
Jun 2026
Last Clinical Review
Not reviewed
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Some fields are incomplete or unverified. If you represent Philips Ultrasound, you can verify and update this listing.
