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
2018507824
Device Listing 2018507824
Listing Summary
#
Listing key
2018507824
Premarket submission
K123983
Device
FASTPACK VITAMIN D; IMMUNOASSAY, CALIBRATORS, CONTROLS, VERIFIERS
Applicant
Qualigen, Inc.
Product code
MRG
Decision date
2013-07-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
57075
2032087
3003355251
QUALIGEN, INC.
1
N
2026-01-01
2042 CORTE DEL NOGAL CARLSBAD CA US 92011