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
1033105188
Device Listing 1033105188
Listing Summary
#
Listing key
1033105188
Premarket submission
K103053
Device
VERIFY 270FP CHALLENGE PACK
Applicant
STERIS Corporation
Product code
JOJ
Decision date
2011-03-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
279796
8021896
3001168737
ALBERT BROWNE LTD.
1
N
2026-01-01
Rayns Way Watermead Business Park Syston LEICESTER GB LE7 1PF
280027
3000251274
3000251274
STERIS Corporation
1
N
2026-01-01
6515 HOPKINS RD. Mentor OH US 44060