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
1567579040
Device Listing 1567579040
Listing Summary
#
Listing key
1567579040
Premarket submission
K250529
Device
Globe Introducer (601-01001)
Applicant
Kardium, Inc.
Product code
DRA
Decision date
2025-06-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
99121
3007603855
3007603855
KARDIUM Inc.
1
N
2026-01-01
8518 Glenlyon Parkway, Unit 155 Burnaby British Columbia CA V5J0B6