YASARGIL SUCTION TUBE - MEDIUM

YASARGIL SUCTION TUBE - MEDIUM is an FDA 510(k)-cleared medical device (K760747) manufactured by Codman & Shurtleff, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 31, 1976. Regulation: 8.