MICROLIFE DUAL MODE THERMOMETER,MODEL IFR1MJ1

MICROLIFE DUAL MODE THERMOMETER,MODEL IFR1MJ1 is an FDA 510(k)-cleared medical device (K113141) manufactured by Microlife Intellectual Property GmbH. 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 January 26, 2012. Regulation: 8.