Epix Electrosurgical Probe with Smoke Evacuation

K151480 is the FDA 510(k) clearance record for Epix Electrosurgical Probe with Smoke Evacuation, a class II device, cleared for Applied Medical Resources on 2016-02-19 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 115 510(k) clearances for Applied Medical Resources, from 1992-12-11 to 2026-04-24. As of 2026-09-10, FDA records show no recalls naming K151480.