Medical Device Manufacturer · IT , Rome

Qualimed Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014

Total

Cleared

Denied

Qualimed Srl has 2 FDA 510(k) cleared medical devices. Based in Rome, IT.

Historical record: 2 cleared submissions from 2014 to 2018. Primary specialty: Ophthalmic.

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

FDA 510(k) Regulatory Record - Qualimed Srl

2 devices

1-2 of 2