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
1582238836
Device Listing 1582238836
Listing Summary
#
Listing key
1582238836
Premarket submission
K862975
Device
MODIFIED PTCA GUIDING CATHETERS
Applicant
Cordis Corp.
Product code
DQY
Decision date
1986-09-23
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