ELECTROSURGICAL PROBES AND DEVICES-GELTX

ELECTROSURGICAL PROBES AND DEVICES-GELTX is an FDA 510(k)-cleared medical device (K002269) manufactured by Ximed/Prosure/Injectx. 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 January 3, 2001. Regulation: 8.