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
1411322928
Device Listing 1411322928
Listing Summary
#
Listing key
1411322928
Premarket submission
K970794
Device
LATEX PATIENT EXAMINATION (POWDERFREE GLOVE)
Applicant
Siam Sempermed Corp., Ltd.
Product code
LYY
Decision date
1997-05-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
91394
3002661124
3002661124
ULINE, INC.
1
Y
2026-01-01
12575 Uline Dr Pleasant Prairie WI US 53158