CRYOPRO MAXI AND CRYOPRO MINI

CRYOPRO MAXI AND CRYOPRO MINI is an FDA 510(k)-cleared medical device (K982280) manufactured by Cortex Technology Aps. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 1998. Regulation: 8.