TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EP

TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EP is an FDA 510(k)-cleared medical device (K993856) manufactured by Tuttnauer U.S.A Co, Ltd.. 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 February 8, 2001. Regulation: 8.