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
1553046710
Device Listing 1553046710
Listing Summary
#
Listing key
1553046710
Premarket submission
K251258
Device
MC2™ Two-Stage Venous Cannula; MC2X™ Three-Stage Venous Cannula
Applicant
Medtronic, Inc.
Product code
DWF
Decision date
2025-06-20
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