Electrosurgical Dispersive Electrode and Electrosurgical Dual Return Electrode with Conductive Gel and 10 Ft. Cord

K940299 is the FDA 510(k) clearance record for ELECTROSURGICAL DISPERSIVE ELECTRODE AND ELECTROSURGICAL DUAL RETURN ELECTRODE WITH CONDUCTIVE GEL AND 10 FT. CORD, a class II device, cleared for Debusk Technology Corp. on 1994-05-02 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 4 510(k) clearances for Debusk Technology Corp., from 1994-03-30 to 1996-07-03. As of 2026-09-10, FDA records show no recalls naming K940299.