Biotek-Caribbean - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Biotek-Caribbean has 1 FDA 510(k) cleared medical devices. Based in Santo Domingo, Dom. Rep., DO.
Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Biotek-Caribbean Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biotek-Caribbean
1 devices