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
1991258623
Device Listing 1991258623
Listing Summary
#
Listing key
1991258623
Premarket submission
K080937
Device
POWDER FREE NITRILE EXAMINATION GLOVE, ORANGE
Applicant
Gx Corporation Sdn Bhd
Product code
LZA
Decision date
2008-05-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17400
9613993
3001856884
Terrell A. Cunningham
1
N
2020-04-25
12812 Meadowbrook Ln. Waldorf MD US 20601