ENDOCARE ELECTROSURGICAL HANDPIECE

ENDOCARE ELECTROSURGICAL HANDPIECE is an FDA 510(k)-cleared medical device (K952698) manufactured by Cytocare, 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 13, 1995. Regulation: 8.