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FDA 510(k) Applications Submitted by CARDEON CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K001371
05/01/2000
CARDEON ASCENDING BALLOON CANNULA (ABC)
CARDEON CORP.
K022042
06/24/2002
MODIFICATION TO CARDEON ASCENDING BALLOON CANNULA (ABC)
CARDEON CORP.
K022174
07/03/2002
MODIFICATION TO CARDEON AEGIS CATHETER
CARDEON CORP.
K042156
08/10/2004
CARDEON COBRA CATHETER
CARDEON CORP.
K013593
10/30/2001
CARDEON AEGIS CATHETER
CARDEON CORP.
K024058
12/09/2002
MODIFICATION TO CARDEON AEGIS CATHETER
CARDEON CORP.
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