PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES

PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES is an FDA 510(k)-cleared medical device (K932392) manufactured by Phx Technologies Corp.. 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 November 21, 1993. Regulation: 8.