ALT-001952K071204Amber Status
C.R. Bard, Inc.
SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6
All identifiers (2)
Aletia (canonical)
ALT-001952FDA 510(k) ยท US (primary)
K071204Regulatory Registrations
๐
US
FDA
ID: K071204
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 C.R. Bard, Inc., you can verify and update this listing.
