STEAM/EO RECORD CARD, MODEL CI 121

STEAM/EO RECORD CARD, MODEL CI 121 is an FDA 510(k)-cleared medical device (K000502) manufactured by Steritec Products Mfg Co, Inc.. 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 March 13, 2000. Regulation: 8.