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
1149000532
Device Listing 1149000532
Listing Summary
#
Listing key
1149000532
Premarket submission
K192722
Device
Padlock Clip defect closure system, Padlock Pro-Select defect closure device
Applicant
STERIS Corporation
Product code
PKL
Decision date
2019-10-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
281663
1528319
1000122656
UNITED STATES ENDOSCOPY GROUP, INC.
1
N
2026-01-01
5976 Heisley Rd Mentor OH US 44060