CIMARRON 1000 OR 1000-2

CIMARRON 1000 OR 1000-2 is an FDA 510(k)-cleared medical device (K790293) manufactured by Cimarron Instruments, 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 April 11, 1979. Regulation: 8.