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
1192307078
Device Listing 1192307078
Listing Summary
#
Listing key
1192307078
Premarket submission
K141951
Device
DLP SILICONE CORONARY ARTERY OSTIAL CANNULAE
Applicant
Medtronic, Inc.
Product code
DWF
Decision date
2014-08-15
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
323251
3003955307
3003955307
Medtronic Grand Rapids
1
N
2026-01-01
620 Watson SW Grand Rapids MI US 49504