Medical Device Manufacturer · US , Palo Alto , CA

Cardiogenes - FDA 510(k) Cleared Devices

20 submissions · 19 cleared · Since 1992
20
Total
19
Cleared
0
Denied

Cardiogenes has 19 FDA 510(k) cleared general & plastic surgery devices. Based in Palo Alto, US.

Historical record: 19 cleared submissions from 1992 to 1997.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cardiogenes

20 devices
1-12 of 20
Filters