PREP TRAY, PREOPERATIVE SKIN

PREP TRAY, PREOPERATIVE SKIN is an FDA 510(k)-cleared medical device (K781797) manufactured by Pharmaseal Div., Baxter Healthcare Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 7, 1978. Regulation: 8.