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
1521962143
Device Listing 1521962143
Listing Summary
#
Listing key
1521962143
Premarket submission
K081260
Device
KIMBERLY-CLARK *LAVENDER* NITRILE POWER-FREE EXAM GLOVES
Applicant
Kimberly-Clark Corp.
Product code
LZA
Decision date
2008-07-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21748
3004059935
3004059935
Michael van der Woude
1
N
2020-04-25
2500 Bee Cave Road Bldg 1, Suite 300 Austin TX US 78746