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
1052312403
Device Listing 1052312403
Listing Summary
#
Listing key
1052312403
Premarket submission
K151611
Device
OneTouch Ultra Plus Flex Blood Glucose Monitoring System
Applicant
Lifescan Europe
Product code
NBW
Decision date
2015-12-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
116559
3008382007
3008382007
LIFESCAN EUROPE GMBH
1
N
2026-01-01
Dammstrasse 19 CH Zug CH 6300