VENI-GARD AP & TPN, DERMA-SHIELD, DERMA-SHIELD JR.

VENI-GARD AP & TPN, DERMA-SHIELD, DERMA-SHIELD JR. is an FDA 510(k)-cleared medical device (K850133) manufactured by Consolidated Medical Equipment, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 27, 1985. Regulation: 8.