tim.hodson
Mon, 09/08/2025 – 14:16
Sept. 4, 2025 — Sentec recently announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its LuMon Electrical Impedance Tomography (EIT) system for premature infant, infant, adolescent and adult patients — making it the first EIT technology in the United States available for premature infants and for spontaneously breathing patients.
While the LuMon System can be used to monitor a variety of patients, whether ve…