IndexMethodologyInsightsFor CliniciansRequest Review
Index/Acuson Corp.
ALT-001327K010950Amber Status

Acuson Corp.

CYPRESS SYSTEM

All identifiers (2)
Aletia (canonical)ALT-001327
FDA 510(k) ยท US (primary)K010950

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K010950
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 Acuson Corp., you can verify and update this listing.
Verify this listing โ†’
โ† Back to Index