SAFETEX & SUNTEX PATIENT EXAMINATION GLOVES

SAFETEX & SUNTEX PATIENT EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K892478) manufactured by P.T. Latexindo Prautama. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 7, 1989. Regulation: 8.