Olympus Psd-20 Electrosurgical System & Its Associated Accessories

K021852 is the FDA 510(k) clearance record for OLYMPUS PSD-20 ELECTROSURGICAL SYSTEM & ITS ASSOCIATED ACCESSORIES, a class II device, cleared for Olympus Optical Co., Ltd. on 2003-02-11 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 48 510(k) clearances for Olympus Optical Co., Ltd., from 1996-11-29 to 2003-10-16. As of 2026-09-10, FDA records show no recalls naming K021852.