RUBICOR BREAST BIOPSY DEVICE

RUBICOR BREAST BIOPSY DEVICE is an FDA 510(k)-cleared medical device (K020047) manufactured by Rubicor 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 April 4, 2002. Regulation: 8.