Bausch Health Americas Incorporated - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bausch Health Americas Incorporated has 1 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bausch Health Americas Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bausch Health Americas Incorporated
1 devices