F.M. Wiest USA, Inc. - FDA 510(k) Cleared Devices

F.M. Wiest USA, Inc. has 12 FDA 510(k) cleared medical devices. Based in Cherry Hill, US.

Historical record: 12 cleared submissions from 1986 to 1994. Primary specialty: Gastroenterology & Urology.

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