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
1753899090
Device Listing 1753899090
Listing Summary
#
Listing key
1753899090
Premarket submission
K111488
Device
MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003
Applicant
Bridgepoint Medical
Product code
DQX
Decision date
2011-06-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
52258
2183870
2183870
ev3, Inc.
1
N
2026-01-01
4600 Nathan Lane North Plymouth MN US 55442