ALT-001199K000338Amber Status
Nihon Kohden America, Inc.
VITAPORT 3
All identifiers (2)
Aletia (canonical)
ALT-001199FDA 510(k) · US (primary)
K000338Regulatory Registrations
🌐
US
FDA
ID: K000338
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 Nihon Kohden America, Inc., you can verify and update this listing.