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
1155901996
Device Listing 1155901996
Listing Summary
#
Listing key
1155901996
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
207078
3005805710
3005805710
Cardinal Health Mexico 514 de RL de CV
1
N
2020-04-25
Presidente masarik 111, Piso 1 Col Polanco V Seccion CP Distrito Federal MX 11560
207079
3013552412
3013552412
Cardinal Health Australia 503 PTY LTD
1
N
2020-04-25
Level 11, 50 Queen Street Melbourne Victoria AU 3000