Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe

K213013 is the FDA 510(k) clearance record for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe, a class II device, cleared for Jeil Tech Co., Ltd. on 2022-09-19 under FDA product code QNQ (Low Dead Space Piston Syringe). FDA's definition for product code QNQ reads: "A low dead space syringe is a piston syringe designed to reduce medication waste. The device consists of a calibrated hollow barrel, a moveable plunger, and may include a needle. The device can be used by health care professions or for...". FDA records list one 510(k) clearance for Jeil Tech Co., Ltd. As of 2026-09-10, FDA records show no recalls naming K213013.