ALT-001333K011204Amber Status
Nihon Kohden America, Inc.
NEUROFAX, MODELS EEG-1100A, EEG-9100A
All identifiers (2)
Aletia (canonical)
ALT-001333FDA 510(k) ยท US (primary)
K011204Regulatory Registrations
๐
US
FDA
ID: K011204
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.
