Promex, Inc. - FDA 510(k) Cleared Devices

Promex, Inc. has 18 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 18 cleared submissions from 1994 to 2002. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Promex, Inc. Filter by specialty or product code using the sidebar.