TUBE, LEATHERMAN/IMBRUCE

TUBE, LEATHERMAN/IMBRUCE is an FDA 510(k)-cleared medical device (K781665) manufactured by National Catheter Co. Div. Mallinckrodt. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 14, 1978. Regulation: 8.