MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES

MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES is an FDA 510(k)-cleared medical device (K884097) manufactured by Circon Acmi. 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 April 16, 1989. Regulation: 8.