Medical Device Manufacturer · IT , Mirandola ( Modena)

Dideco - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Dideco has 5 FDA 510(k) cleared medical devices. Based in Mirandola ( Modena), IT.

Historical record: 5 cleared submissions from 1995 to 2001. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Dideco

5 devices

1-5 of 5