Siemens Radiotom 904 & 904E Electrosurgery Unit

K912070 is the FDA 510(k) clearance record for SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT, a class II device, cleared for Siemens Medical Electronics on 1992-04-23 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 15 510(k) clearances for Siemens Medical Electronics, from 1988-07-18 to 1995-04-07. As of 2026-09-10, FDA records show no recalls naming K912070.