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
1305591525
Device Listing 1305591525
Listing Summary
#
Listing key
1305591525
Premarket submission
K093759
Device
MULTIPLE NAME MODEL MULTIPLE
Applicant
Gx Corporation Sdn Bhd (Plant 1)
Product code
LZA
Decision date
2010-02-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
75653
3004941385
3004941385
Terrell A. Cunningham
1
N
2020-04-25
12812 Meadowbrook Ln. Waldorf MD US 20601