ALT-001220K001306Amber Status
Andromed, Inc.
STETHOS, MODEL STXXYYZZ OR 001 XXX, STETHOS LINK, MODEL SLXXYYZZ OR 002 XXX
All identifiers (2)
Aletia (canonical)
ALT-001220FDA 510(k) ยท US (primary)
K001306Regulatory Registrations
๐
US
FDA
ID: K001306
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 Andromed, Inc., you can verify and update this listing.
