DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P

DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P is an FDA 510(k)-cleared medical device (K792273) manufactured by Dexide, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 9, 1979. Regulation: 8.