ALT-001534K030962Amber Status
Ge Lunar Corp.
DPX SERIES BRAVO DUO BONE DENSITOMETER
All identifiers (2)
Aletia (canonical)
ALT-001534FDA 510(k) ยท US (primary)
K030962Regulatory Registrations
๐
US
FDA
ID: K030962
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 Ge Lunar Corp., you can verify and update this listing.
