Model I 100 RF Passive Attenuator/splitter and Model Ql 10 Loop Electrode

K964779 is the FDA 510(k) clearance record for MODEL I 100 RF PASSIVE ATTENUATOR/SPLITTER AND MODEL QL 10 LOOP ELECTRODE, a class II device, cleared for Quantum Loop, Inc. on 1997-08-27 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 one 510(k) clearance for Quantum Loop, Inc. As of 2026-09-10, FDA records show no recalls naming K964779.