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
1758710834
Device Listing 1758710834
Listing Summary
#
Listing key
1758710834
Premarket submission
K073683
Device
VERIFY CHALLENGE PACKS - VERSION 2
Applicant
STERIS Corporation
Product code
JOJ
Decision date
2008-01-25
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