Ethox International is one of 14510 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ethox International - FDA 510(k) Cleared Devices
Recent clearances: SURGI-CUF REUSABLE, RS SERIES
1
Total
1
Cleared
0
Denied
Ethox International has 1 FDA 510(k) cleared medical devices. Based in Buffalo, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ethox International Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Ethox International
1 devices