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
1507423446
Device Listing 1507423446
Listing Summary
#
Listing key
1507423446
Premarket submission
K091022
Device
MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT
Applicant
STERIS Corporation
Product code
MED
Decision date
2010-04-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
335073
3034286426
1937223
CIVCO Medical Instruments Co., Inc.
1
N
2026-01-01
750 Lois Lane Coralville IA US 52241