IndexMethodologyInsightsFor CliniciansFor RegulatorsRequest Review
Index/Philips Ultrasound
ALT-006651K223771Green Status

Lumify Diagnostic Ultrasound System

Philips Ultrasound · Manufacturer

All identifiers (4)
Aletia (canonical)ALT-006651
FDA 510(k) · US (primary)K223771
FDA 510(k) · USK252557
FDA 510(k) · USK232500

Overview

Accountability Tier
Tier 2

Regulatory Registrations

🌐
US
FDA
ID: K223771
510k

Lifecycle Signals

Last Automated Sync
Jun 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, you can verify and update this listing.
Verify this listing →
← Back to Index