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
1928826601
Device Listing 1928826601
Listing Summary
#
Listing key
1928826601
Premarket submission
K782048
Device
TEST KIT, IIF-ANA
Applicant
Medica Corp.
Product code
DHN
Decision date
1979-01-17
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