LATEX EXAMINATION GLOVES, STYLE 510 LX

LATEX EXAMINATION GLOVES, STYLE 510 LX is an FDA 510(k)-cleared medical device (K891418) manufactured by C & K Mfg. & Sales Co.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1989. Regulation: 8.