Ethox Corp. - FDA 510(k) Cleared Devices

Ethox Corp. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1977 to 2004. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Entela, Inc. as regulatory consultant.