Neuroview Coaxial Bipolar Electrode

K955467 is the FDA 510(k) clearance record for NEUROVIEW COAXIAL BIPOLAR ELECTRODE, a class II device, cleared for Neuro Navigational Corp. on 1995-12-18 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 23 510(k) clearances for Neuro Navigational Corp., from 1993-01-29 to 1997-03-06. As of 2026-09-10, FDA records show no recalls naming K955467.