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
1261020590
Device Listing 1261020590
Listing Summary
#
Listing key
1261020590
Premarket submission
K112250
Device
CHX=CHX PLUS
Applicant
Inter-Med, Inc.
Product code
KJJ
Decision date
2011-10-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
52282
2133714
3000209941
INTER-MED, INC.
1
N
2026-01-01
2200 South St Racine WI US 53404