Drug news
FDA gives 510(K) approval of the MicroThermX Microwave Ablation System for laparoscopic ablation-Perseon Corp
Perseon Corporation has announced that the company received additional 510(K) clearance from the FDA to market the MicroThermX Microwave Ablation System (MicroThermX) for the specific indication of laparoscopic ablation procedures using image guidance. The MicroThermX is a compact, mobile, state-of-the-art, proprietary system that includes a microwave generator, single-patient-use disposable antennas, and a thermistor-based temperature monitoring system. The design of the MicroThermX is the first of its kind that allows delivery of higher power levels using a single generator.
The company already has 510(k) clearance to market the MicroThermX for ablation of soft tissue and has also received CE Marking for the MicroThermX System in the EU.