ALT-001991K072353Amber Status
Dyansys Corp
PORTABLE ECSCOPE
All identifiers (2)
Aletia (canonical)
ALT-001991FDA 510(k) ยท US (primary)
K072353Regulatory Registrations
๐
US
FDA
ID: K072353
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 Dyansys Corp, you can verify and update this listing.
