OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER

OLYMPUS EU-M30 ENDOSCOPIC ULTRASOUND CENTER is an FDA 510(k)-cleared medical device (K951994) manufactured by Olympus America, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 14, 1996. Regulation: 8.