Neuro-Endoscope System by Hopf, Existing of: Endoscopes, Sheaths, Working Elements, Bipolar and Unipolar Electrodes

K031858 is the FDA 510(k) clearance record for NEURO-ENDOSCOPE SYSTEM BY HOPF, EXISTING OF: ENDOSCOPES, SHEATHS, WORKING ELEMENTS, BIPOLAR AND UNIPOLAR ELECTRODES, a class II device, cleared for Richard Wolf Medical Instruments Corp. on 2004-07-29 under FDA product code GWG (Endoscope, Neurological). FDA's definition for product code GWG reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corp., from 1977-03-07 to 2024-06-03. As of 2026-09-10, FDA records show no recalls naming K031858.