UNI-LAB PATIENT EXAMINATION GLOVES (LATEX)

UNI-LAB PATIENT EXAMINATION GLOVES (LATEX) is an FDA 510(k)-cleared medical device (K892486) manufactured by Unicable. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 12, 1989. Regulation: 8.