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
1742881159
Device Listing 1742881159
Listing Summary
#
Listing key
1742881159
Premarket submission
K890048
Device
QUIK-DOT TOXOPLASMOSIS
Applicant
Ampcor, Inc.
Product code
LLA
Decision date
1989-06-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
43497
2247139
1000122189
SCIMEDX CORP.
1
N
2020-04-25
53 Richboynton Rd Dover NJ US 07801