Adaptable Monopolar Adaptable And/or Retractable Electrodes

K062047 is the FDA 510(k) clearance record for ADAPTABLE MONOPOLAR ADAPTABLE AND/OR RETRACTABLE ELECTRODES, a class II device, cleared for PAJUNK GmbH Medizintechnologie on 2006-10-05 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 63 510(k) clearances for PAJUNK GmbH Medizintechnologie, from 1991-10-21 to 2025-07-01. As of 2026-09-10, FDA records show no recalls naming K062047.