OXFORD OPTRONIX MPM 3S

OXFORD OPTRONIX MPM 3S is an FDA 510(k)-cleared medical device (K914397) manufactured by Dia-Stron, Ltd.. 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 November 15, 1992. Regulation: 8.