Medical Device Manufacturer · US , Cupertino , CA

Cardeon Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2000

Total

Cleared

Denied

Cardeon Corp. has 6 FDA 510(k) cleared medical devices. Based in Cupertino, US.

Historical record: 6 cleared submissions from 2000 to 2004. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cardeon Corp. Filter by specialty or product code using the sidebar.

Cardeon Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cardeon Corp.

6 devices

1-6 of 6