MODEL GT1ST CRYOSURGICAL INSTRUMENT

MODEL GT1ST CRYOSURGICAL INSTRUMENT is an FDA 510(k)-cleared medical device (K922878) manufactured by Gyne-Tech Instrument Corp.. 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 September 1, 1992. Regulation: 8.