
J.J. Skinner, Inc.
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CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS is an FDA 510(k)-cleared medical device (K903544) manufactured by J.J. Skinner, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 30, 1990. Regulation: 8.