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
1651424905
Device Listing 1651424905
Listing Summary
#
Listing key
1651424905
Premarket submission
K181592
Device
RAIN Sheath Transradial
Applicant
Cordis Corporation
Product code
DYB
Decision date
2018-08-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17
1016427
1016427
Cordis US Corp.
1
Y
2026-01-01
14201 N.W. 60TH AVE. Miami Lakes FL US 33014
16
9616099
3003528016
Linda Ruedy
1
N
2026-01-01
5452 Betsy Ross Dr Santa Clara CA US 95054