RIGID FIBEROPITC ENDOSCOPE

RIGID FIBEROPITC ENDOSCOPE is an FDA 510(k)-cleared medical device (K844769) manufactured by Microvasive. 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 January 14, 1985. Regulation: 8.