IndexMethodologyInsightsFor CliniciansFor RegulatorsRequest Review
Index/Philips Ultrasound LLC
ALT-006392K242020Green Status

EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System

Philips Ultrasound LLC · Manufacturer

All identifiers (7)
Aletia (canonical)ALT-006392
FDA 510(k) · US (primary)K242020
FDA 510(k) · USK251651
FDA 510(k) · USK243794
FDA 510(k) · USK250177
FDA 510(k) · USK243793
FDA 510(k) · USK251455

Overview

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.
Verify this listing →
← Back to Index