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
1089991242
Device Listing 1089991242
Listing Summary
#
Listing key
1089991242
Premarket submission
K993720
Device
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER
Applicant
Cordis Corp.
Product code
KNQ
Decision date
2000-01-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3008
1047843
1047843
ISOMEDIX OPERATIONS INC.
1
N
2026-01-01
2072 Southport Rd SPARTANBURG SC US 29306
3006
1643817
1643817
ISOMEDIX OPERATIONS INC
1
N
2026-01-01
1435 ISOMEDIX PLACE EL PASO TX US 79936