Lancet, Blood

K883420 is the FDA 510(k) clearance record for LANCET, BLOOD, a class II device, cleared for Primrose Medical, Inc. on 1988-08-26 under FDA product code FMK (Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature). FDA's definition for product code FMK reads: "A disposable blood lancet intended for a single use that is comprised of a single use blade attached to a solid, non-reusable base (including an integral sharps injury prevention feature) that is used to puncture the skin to obtain a drop...". FDA records list 14 510(k) clearances for Primrose Medical, Inc., from 1984-08-24 to 1989-09-29. As of 2026-09-10, FDA records show no recalls naming K883420.