ALT-001943K070907Amber Status
Regulatory Management Services
INTERSON USB ULTRASOUND PROBE SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001943FDA 510(k) · US (primary)
K070907Regulatory Registrations
🌐
US
FDA
ID: K070907
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 Regulatory Management Services, you can verify and update this listing.