
Cryosurg, Inc.
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VERRUCA-FREEZE(TM) CRYOTHERAPY DELIVERY SYSTEM is an FDA 510(k)-cleared medical device (K881349) manufactured by Cryosurg, Inc.. 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 June 29, 1988. Regulation: 8.