IndexMethodologyInsightsFor CliniciansFor RegulatorsRequest Review
Index/Philips Ultrasound, Inc.
ALT-006996K201012Green Status

EPIQ Diagnostic Ultrasound System Series, Affiniti Diagnostic Ultrasound System Series, CX50 Diagnostic Ultrasound System, Sparq Diagnostic Ultrasound System, Lumify Diagnostic Ultrasound System

Philips Ultrasound, Inc. ยท Manufacturer

All identifiers (2)
Aletia (canonical)ALT-006996
FDA 510(k) ยท US (primary)K201012

Overview

Accountability Tier
Tier 2

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K201012
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, Inc., you can verify and update this listing.
Verify this listing โ†’
โ† Back to Index