14G CORMARK BIOPSY SITE IDENTIFIER

14G CORMARK BIOPSY SITE IDENTIFIER is an FDA 510(k)-cleared medical device (K032217) manufactured by Artemis Medical, 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 August 20, 2003. Regulation: 8.