Eschmann Electrosurgical Unit, Model Td411

K852935 is the FDA 510(k) clearance record for ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411, a class II device, cleared for Eschmann Bros. & Walsh , Ltd. on 1985-10-10 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 3 510(k) clearances for Eschmann Bros. & Walsh , Ltd., from 1978-11-06 to 1987-01-06. As of 2026-09-10, FDA records show no recalls naming K852935.