ALT-006392K242020Green Status
EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System
Philips Ultrasound LLC · Manufacturer
All identifiers (7)
Aletia (canonical)
ALT-006392FDA 510(k) · US (primary)
K242020FDA 510(k) · US
K251651FDA 510(k) · US
K243794FDA 510(k) · US
K250177FDA 510(k) · US
K243793FDA 510(k) · US
K251455Overview
Accountability Tier
Tier 2
Regulatory Registrations
🌐
US
FDA
ID: K242020
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 LLC, you can verify and update this listing.
