OLYMPUS ULTRASONIC PROBE FOR ESOPHOGUS (MH-908)

OLYMPUS ULTRASONIC PROBE FOR ESOPHOGUS (MH-908) is an FDA 510(k)-cleared medical device (K952892) 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 February 11, 1996. Regulation: 8.