SENSI-DERM LATEX SURGICAL GLOVES (POWDERED)

SENSI-DERM LATEX SURGICAL GLOVES (POWDERED) is an FDA 510(k)-cleared medical device (K980880) manufactured by Ansell Perry. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 19, 1998. Regulation: 8.