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
1607565681
Device Listing 1607565681
Listing Summary
#
Listing key
1607565681
Premarket submission
K162098
Device
LED Phototherapy Device
Applicant
Li-Tek Electronic Technology Corporation
Product code
OLP
Decision date
2017-01-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
33488
1832894
1832894
FKA Distributing Co., LLC
1
Y
2026-01-01
3000 N Pontiac Trl Commerce Township MI US 48390