STINGRAY ELECTROSURGICAL FORCEPS

STINGRAY ELECTROSURGICAL FORCEPS is an FDA 510(k)-cleared medical device (K083162) manufactured by Stingray Surgical Products, 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 January 11, 2009. Regulation: 8.