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
1243150591
Device Listing 1243150591
Listing Summary
#
Listing key
1243150591
Premarket submission
K001050
Device
CALCIJECT
Applicant
Centrix, Inc.
Product code
EJK
Decision date
2000-07-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
30768
1281412
1281412
CENTRIX, INC.
1
Y
2026-01-01
770 River Rd Shelton CT US 06484