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
1966490385
Device Listing 1966490385
Listing Summary
#
Listing key
1966490385
Premarket submission
K974131
Device
ALERT
Applicant
Jeneric/Pentron, Inc.
Product code
EBF
Decision date
1997-12-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
340662
3038718579
3038718579
OKETZ LOGISTICS LLC
1
Y
2026-01-01
50 Minorca Ave Coral Gables FL US 33134