NETHERY EXTREMITY FREEZING UNIT

NETHERY EXTREMITY FREEZING UNIT is an FDA 510(k)-cleared medical device (K844246) manufactured by Howard J. Nethery & Assoc.. 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 February 27, 1985. Regulation: 8.