Shinmed Various Models of Electro-Surgical Pencils, Sw12200, Sw12202, Sw12300

K033027 is the FDA 510(k) clearance record for SHINMED VARIOUS MODELS OF ELECTRO-SURGICAL PENCILS, SW12200, SW12202, SW12300, a class II device, cleared for Shining World Health Care Co., Ltd. on 2004-08-12 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 Shining World Health Care Co., Ltd., from 1999-09-03 to 2022-01-28. As of 2026-09-10, FDA records show no recalls naming K033027.