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
1439618722
Device Listing 1439618722
Listing Summary
#
Listing key
1439618722
Premarket submission
K980088
Device
T-UPTAKE MICROPLATE EIA
Applicant
Monobind
Product code
KHQ
Decision date
1998-02-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
50079
2029372
1000306617
Diagnostic Automation/ Cortez Diagnostics Inc,.
1
Y
2026-01-01
21250 Califa St Suite 102 and 116 Woodland Hills CA US 91367