Medical Device Manufacturer · FR , 21300 Chenove

Laboratoires Urgo - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2006

Total

Cleared

Denied

Laboratoires Urgo has 6 FDA 510(k) cleared medical devices. Based in 21300 Chenove, FR.

Historical record: 6 cleared submissions from 2006 to 2015. Primary specialty: General & Plastic Surgery.

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

Laboratoires Urgo is one of 160 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Laboratoires Urgo

6 devices

1-6 of 6