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
1712664779
Device Listing 1712664779
Listing Summary
#
Listing key
1712664779
Premarket submission
P950008
Device
SILIKON 1000
Applicant
ALCON
Product code
LWL
Decision date
1997-09-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3069
1610287
1610287
Alcon Research, LLC
1
Y
2026-01-01
6201 SOUTH FREEWAY Fort Worth TX US 76134