ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA

ADAIR INSUFFLATION AND INSTRUMENTATION CANNULA is an FDA 510(k)-cleared medical device (K936155) manufactured by Micromedical Devices, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 10, 1994. Regulation: 8.