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Company-Registration
1996256701
Device Listing 1996256701
Listing Summary
#
Listing key
1996256701
Premarket submission
K121442
Device
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
Applicant
Cordis Corporation
Product code
LIT
Decision date
2012-06-14
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
205259
3013510102
3013510102
CARDINAL HEALTH IRELAND UNLIMITED C/O ARVATO BENELUX BV
1
N
2020-04-25
30 BREM 1 Gennep Limburg NL 6598 MH