PLASTIC FORCEPS CAT.#1001-1010

PLASTIC FORCEPS CAT.#1001-1010 is an FDA 510(k)-cleared medical device (K801991) manufactured by Pollak (Intl.), Ltd.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 15, 1980. Regulation: 8.