Modification to Autocon II 400 Electrosurgical Generator

K062464 is the FDA 510(k) clearance record for MODIFICATION TO AUTOCON II 400 ELECTROSURGICAL GENERATOR, a class II device, cleared for KARL STORZ Endoscopy-America, Inc. on 2007-02-16 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 402 510(k) clearances for KARL STORZ Endoscopy-America, Inc., from 1980-04-21 to 2026-05-15. As of 2026-09-10, FDA records show no recalls naming K062464.