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
1371236137
Device Listing 1371236137
Listing Summary
#
Listing key
1371236137
Premarket submission
K113853
Device
G+ SYSTEM
Applicant
Glytec, LLC
Product code
NDC
Decision date
2012-05-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
67067
3005853093
3005853093
Glytec, LLC
1
N
2026-01-01
220 N Main St Greenville SC US 29601