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
1979209146
Device Listing 1979209146
Listing Summary
#
Listing key
1979209146
Premarket submission
K842383
Device
PATHO DX LATEX AGGLUTINATION STREP A
Applicant
Diagnostic Products Corp.
Product code
GTZ
Decision date
1984-07-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
7642
3003750284
3003750284
Joel Mathew
1
N
2026-01-01
12076 Santa Fe Trail Lenexa KS US 66215