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
1290285430
Device Listing 1290285430
Listing Summary
#
Listing key
1290285430
Premarket submission
K103574
Device
PREGNANCY ONE STEP RAPID TEST
Applicant
Lehnus & Associates Consulting
Product code
LCX
Decision date
2011-07-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
250152
0
0
VERIFY DIAGNOSTICS
5
N
2020-04-25
D-122 Commerce Park Dr Barrie Ontario CA L4N 8W8