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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact