
F.M. Wiest USA, Inc.
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F.M. WEIST,KG (URODYNAMIC SYSTEMS) is an FDA 510(k)-cleared medical device (K860571) manufactured by F.M. Wiest USA, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 17, 1986. Regulation: 8.