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
1700573975
Device Listing 1700573975
Listing Summary
#
Listing key
1700573975
Premarket submission
K152789
Device
FLEX SCORING CATHETER
Applicant
Venturemed Group
Product code
PNO
Decision date
2016-05-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
195172
3012696653
3012696653
VENTUREMED GROUP, Inc
1
N
2026-01-01
2800 Campus Dr. Suite 50 Plymouth MN US 55441