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
1196545049
Device Listing 1196545049
Listing Summary
#
Listing key
1196545049
Premarket submission
K993147
Device
DECAP
Applicant
The Kipp Group
Product code
FPA
Decision date
1999-11-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
256720
3012410077
3012410077
CAREFUSION
1
Y
2026-01-01
3750 Torrey View Court San Diego CA US 92130