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
1642649639
Device Listing 1642649639
Listing Summary
#
Listing key
1642649639
Premarket submission
K060778
Device
SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWDER FREE
Applicant
Ever Light Plastic Products Co., Ltd.
Product code
LYZ
Decision date
2006-04-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
24761
3005596481
3005596481
Kathy Liu
1
N
2026-01-01
3973 Schaefer Avenue Chino CA US 91710