SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES

SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES is an FDA 510(k)-cleared medical device (K052692) manufactured by Suretek Medical. 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 May 9, 2006. Regulation: 8.