MOD. MCI 17 MANUAL CUFF INFLATOR

MOD. MCI 17 MANUAL CUFF INFLATOR is an FDA 510(k)-cleared medical device (K800767) manufactured by Medasonics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 23, 1980. Regulation: 8.