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
1821226846
Device Listing 1821226846
Listing Summary
#
Listing key
1821226846
Premarket submission
K021566
Device
INFINITI
Applicant
Alcon Laboratories, Inc.
Product code
HQC
Decision date
2002-07-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
4374
1928237
1928237
MIDWEST STERILIZATION CORP.
1
N
2026-01-01
1204 LENCO AVE. JACKSON MO US 63755