Duraprene Sterile Synthetic Powder-Free Surgical Gloves with Tested for Use with Chemotherapy Drugs Labeling Claim

K013302 is the FDA 510(k) clearance record for DURAPRENE STERILE SYNTHETIC POWDER-FREE SURGICAL GLOVES WITH TESTED FOR USE WITH CHEMOTHERAPY DRUGS LABELING CLAIM, a class I device, cleared for Allegiance Healthcare Corp. on 2001-12-17 under FDA product code KGO (Surgeon'S Gloves). FDA's definition for product code KGO reads: "A surgeon's glove is a disposable device made of natural rubber latex or synthetic polymers that may or may not bear powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a...". FDA records list 1,525 510(k) clearances for Medtronic, Inc., from 1976-08-23 to 2026-08-13. As of 2026-09-10, FDA records show no recalls naming K013302.