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
2020112887
Device Listing 2020112887
Listing Summary
#
Listing key
2020112887
Premarket submission
K192292
Device
L10 LED Light Source with AIM, L11 LED Light Source with AIM, AIM SafeLight Cable
Applicant
Stryker
Product code
OWN
Decision date
2019-11-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3775
2936485
2936485
STRYKER ENDOSCOPY
1
N
2026-01-01
5900 Optical Ct SAN JOSE CA US 95138