Satari Latex Patient Examination Powdered Glove Single Side Polymer Coated, Non Sterile, 200 Mg or Less of Total Water E

K014112 is the FDA 510(k) clearance record for SATARI LATEX PATIENT EXAMINATION POWDERED GLOVE SINGLE SIDE POLYMER COATED, NON STERILE, 200 MG OR LESS OF TOTAL WATER E, a class I device, cleared for Siam Sempermed Corp., Ltd. on 2002-02-28 under FDA product code LYY (Latex Patient Examination Glove). FDA's definition for product code LYY reads: "A latex patient examination glove is a disposable device made of natural rubber latex that may or may not bear a trace amount of residual powder, and is intended to be worn on the hand for medical purposes to provide a barrier against...". FDA records list 37 510(k) clearances for Siam Sempermed Corp., Ltd., from 1989-12-05 to 2015-02-11. As of 2026-09-10, FDA records show no recalls naming K014112.