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
1152239463
Device Listing 1152239463
Listing Summary
#
Listing key
1152239463
Premarket submission
K982281
Device
SERAQUEST RUBELLA IGM
Applicant
Quest Intl., Inc.
Product code
LFX
Decision date
1998-10-16
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