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
1763190854
Device Listing 1763190854
Listing Summary
#
Listing key
1763190854
Premarket submission
K021999
Device
GRIPPER PLUS NEEDLE
Applicant
Deltec, Inc.
Product code
FPA
Decision date
2002-08-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
196344
3011088743
3011088743
Zvi Sklarz
1
N
2026-01-01
500 Davistown Rd Blackwood NJ US 08012