Non/gel Fully Adhesive Dispersive Electrode 3428,

K851305 is the FDA 510(k) clearance record for NON/GEL FULLY ADHESIVE DISPERSIVE ELECTRODE 3428,, a class II device, cleared for Richards Medical Co., Inc. on 1985-09-06 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 71 510(k) clearances for Richards Medical Co., Inc., from 1983-09-29 to 1990-06-25. As of 2026-09-10, FDA records show no recalls naming K851305.