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
1900770799
Device Listing 1900770799
Listing Summary
#
Listing key
1900770799
Premarket submission
K834352
Device
ADULT VENT CATHETER
Applicant
Dlp, Inc.
Product code
DRA
Decision date
1984-01-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
5792
2184009
1000116158
MEDTRONIC PERFUSION SYSTEMS
1
N
2026-01-01
7611 Northland Dr Minneapolis MN US 55428
5793
9617601
3002534070
Celia Encinas
1
N
2026-01-01
1610 Landmark Rd San Diego CA US 92154
323251
3003955307
3003955307
Medtronic Grand Rapids
1
N
2026-01-01
620 Watson SW Grand Rapids MI US 49504