
United States Surgical, A Division of Tyco Healthc
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MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC is an FDA 510(k)-cleared medical device (K901107) manufactured by United States Surgical, A Division of Tyco Healthc. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 8, 1990. Regulation: 8.