Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1127251526
Device Listing 1127251526
Listing Summary
#
Listing key
1127251526
Premarket submission
K232501
Device
AI Platform (AIP001)
Applicant
Exo, Inc.
Product code
QIH
Decision date
2023-11-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
305373
3017487805
3017487805
Exo Imaging, Inc.
1
N
2026-01-01
4201 Burton Drive Santa Clara CA US 95054