POREX ELECTROSURGERY NEEDLE

POREX ELECTROSURGERY NEEDLE is an FDA 510(k)-cleared medical device (K052297) manufactured by Porex Surgical, 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 March 27, 2006. Regulation: 8.