SANICLAVE 102, MODEL RS-SC-102

SANICLAVE 102, MODEL RS-SC-102 is an FDA 510(k)-cleared medical device (K122978) manufactured by Alternative Pioneering Research and Development. 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 May 22, 2013. Regulation: 8.