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
1886921781
Device Listing 1886921781
Listing Summary
#
Listing key
1886921781
Premarket submission
K142567
Device
RETeval Visual Electrodiagnostic Device
Applicant
Lkc Technologies, Inc.
Product code
GWE
Decision date
2015-05-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
29534
1119189
1119189
LKC TECHNOLOGIES, INC.
1
N
2026-01-01
20501 Seneca Meadows Pkwy Ste 305 Germantown MD US 20876