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
1350740357
Device Listing 1350740357
Listing Summary
#
Listing key
1350740357
Premarket submission
K132890
Device
SUPRAPUBIC CATHETER AND INTRODUCER SET
Applicant
Mediplus , Ltd.
Product code
KOB
Decision date
2014-01-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
176082
3011308139
3011308139
MEDIPLUS MANUFACTURING LTD.
1
N
2020-04-25
Unit 8 The Gateway Centre, Cressex Business Park Coronation Road Coronation Road Buckinghamshire GB HP12 3SU