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
2019960963
Device Listing 2019960963
Listing Summary
#
Listing key
2019960963
Premarket submission
K232589
Device
Horos MD™
Applicant
Icat Solutions, Ltd.
Product code
LLZ
Decision date
2024-01-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
325128
3030446518
3030446518
ICAT SOLUTIONS LTD
1
N
2026-01-01
51-59 Rose Lane Norwich Norfolk GB NR1 1BY