Laboratoires Urgo S.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laboratoires Urgo S.A. - FDA 510(k) Cleared Devices
2
Total
1
Cleared
0
Denied
Laboratoires Urgo S.A. has 1 FDA 510(k) cleared medical devices. Based in St Louis, US.
Historical record: 1 cleared submissions from 1997 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Laboratoires Urgo S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laboratoires Urgo S.A.
2 devices