RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY

RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY is an FDA 510(k)-cleared medical device (K902092) manufactured by Critikon Company, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 25, 1990. Regulation: 8.