IndexMethodologyInsightsFor CliniciansRequest Review
Index/PAJUNK GmbH Medizintechnologie
ALT-001863K060808Amber Status

PAJUNK GmbH Medizintechnologie

BRAINPRO, BRAINPRO ACCESS

All identifiers (2)
Aletia (canonical)ALT-001863
FDA 510(k) ยท US (primary)K060808

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K060808
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 PAJUNK GmbH Medizintechnologie, you can verify and update this listing.
Verify this listing โ†’
โ† Back to Index