Medical Device Manufacturer · US , Washington , DC

Pronosco A/S - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Total

Cleared

Denied

Pronosco A/S has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 2000 to 2000. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Pronosco A/S Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pronosco A/S

2 devices

1-2 of 2