Midas Touch Electrosurgical Electrode

K973234 is the FDA 510(k) clearance record for MIDAS TOUCH ELECTROSURGICAL ELECTRODE, a class II device, cleared for Iti Medical Technologies, Inc. on 1997-10-27 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 2 510(k) clearances for Iti Medical Technologies, Inc., from 1997-10-27 to 1998-09-08. As of 2026-09-10, FDA records show 2 recalls naming K973234.