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
1096138304
Device Listing 1096138304
Listing Summary
#
Listing key
1096138304
Premarket submission
K945885
Device
PATIENT EXAMINATION GLOVES
Applicant
Hartalega Sdn Bhd
Product code
LYY
Decision date
1995-03-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
41671
8040614
3002807146
HARTALEGA SDN BHD
1
N
2026-01-01
No 7, Kawasan Perusahaan Suria Bestari Jaya Selangor MY 45600