Medical Device Manufacturer · US , Cupertino , CA

Cardeon Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2000

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cardeon Corp. Cardiovascular ✕

6 devices

1-6 of 6

Cleared Oct 06, 2004

CARDEON COBRA CATHETER

Cardiovascular · 57d

Cleared Dec 30, 2002

MODIFICATION TO CARDEON AEGIS CATHETER

Cardiovascular · 21d

Cleared Sep 03, 2002

MODIFICATION TO CARDEON ASCENDING BALLOON CANNULA (ABC)

Cardiovascular · 71d

Cleared Jul 29, 2002

MODIFICATION TO CARDEON AEGIS CATHETER

Cardiovascular · 26d

Cleared Jun 24, 2002

CARDEON AEGIS CATHETER

Cardiovascular · 237d

Cleared Jul 07, 2000

CARDEON ASCENDING BALLOON CANNULA (ABC)

Cardiovascular · 67d