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
1221611149
Device Listing 1221611149
Listing Summary
#
Listing key
1221611149
Premarket submission
K983268
Device
MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAY
Applicant
Diagnostic Reagents, Inc.
Product code
LFH
Decision date
1998-11-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
172291
3010939897
3010939897
Microgenics Corporation
1
Y
2026-01-01
46500 Kato Road Fremont CA US 94538