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
1197317826
Device Listing 1197317826
Listing Summary
#
Listing key
1197317826
Premarket submission
K043443
Device
ONE STEP HCG URINE PREGNANCY TEST
Applicant
Guangzhou Wondfo Biotech Co., Ltd.
Product code
LCX
Decision date
2005-04-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
132618
3006305917
3006305917
AMERICAN SCREENING CORPORATION
1
N
2020-04-25
9742 St. Vincent Street , Suite 100 Shreveport LA US 71106