Patient Examination Gloves (Poly)

K892768 is the FDA 510(k) clearance record for PATIENT EXAMINATION GLOVES (POLY), a class I device, cleared for Promedica Products, Inc. on 1989-06-14 under FDA product code LZA (Polymer Patient Examination Glove). FDA's definition for product code LZA reads: "A nitrile (or polymer) patient examination glove is a disposable device made of nitrile rubber or synthetic polymers 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...". FDA records list 6 510(k) clearances for Promedica Products, Inc., from 1988-08-10 to 1992-08-12. As of 2026-09-10, FDA records show no recalls naming K892768.