CHAMP-PAQ LATEX PATIENT EXAM GLOVES

CHAMP-PAQ LATEX PATIENT EXAM GLOVES is an FDA 510(k)-cleared medical device (K892243) manufactured by Champ-Paq Instrument Corp.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 20, 1989. Regulation: 8.