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
1611364839
Device Listing 1611364839
Listing Summary
#
Listing key
1611364839
Premarket submission
K930849
Device
VERIFY REFERENCE PLASMA AND MDA VERIFY REF. PLASMA
Applicant
Organon Teknika Corp.
Product code
JPA
Decision date
1993-04-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
117413
3008386529
3008386529
Donald Kraft
1
N
2026-01-01
5 Century Dr Parsippany Parsippany NJ US 07054