LEEDAR (PATIENT EXAMINATION GLOVES - LATEX)

LEEDAR (PATIENT EXAMINATION GLOVES - LATEX) is an FDA 510(k)-cleared medical device (K891663) manufactured by Darchet (Usa), Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 12, 1990. Regulation: 8.