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
1060287373
Device Listing 1060287373
Listing Summary
#
Listing key
1060287373
Premarket submission
K983067
Device
FINE-JECT
Applicant
Henke Sass Wolf of America, Inc.
Product code
FMI
Decision date
1998-10-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
69828
8010674
6064
Kamaal Anas
1
N
2026-01-01
824 Twelfth Avenue Bethlehem PA US 18018