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
1140740102
Device Listing 1140740102
Listing Summary
#
Listing key
1140740102
Premarket submission
K915203
Device
D-DIMER WELLCOTEST (HA10)
Applicant
Wellcome Diagnostics
Product code
DAP
Decision date
1992-01-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
7642
3003750284
3003750284
Joel Mathew
1
N
2026-01-01
12076 Santa Fe Trail Lenexa KS US 66215