IndexMethodologyInsightsFor CliniciansRequest Review
Index/Philips Ultrasound, Inc.
ALT-001681K042540Amber Status

Philips Ultrasound, Inc.

PHILIPS IU22 ULTRASOUND SYSTEM

All identifiers (2)
Aletia (canonical)ALT-001681
FDA 510(k) ยท US (primary)K042540

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K042540
510k

Lifecycle Signals

Last Automated Sync
Mar 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