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Radiance 330 Single Room System Receives FDA 510(k) Clearance

ProTom International Holding Corporation ("ProTom"), a market-leading proton therapy technology manufacturer, announced that it has received 510(k) clearance from the U.S. Food and Drug Administration ("FDA") for its Radiance 330 proton therapy system installed at Massachusetts General Hospital ("MGH") in Boston, Massachusetts.

The Radiance 330 proton therapy system at MGH is a compact, single room system equipped with an advanced pencil beam scanning system and integrated imaging and control system. The Radiance 330 compact synchrotron can be installed within an interior accelerator vault space of 20′ x 30′ and requires up to 40% less radiation shielding.

By using the advanced pencil beam scanning technology, modular designed treatment system and the compact synchrotron particle accelerator, Radiance 330 is a smaller, lighter and cleaner system.

About Mass General Hospital

Mass General Hospital is the original and the largest teaching hospital of Harvard Medical School located in Boston, Massachusetts.

Mass General has long been a leader in successfully bridging innovative science with highly advanced clinical medicine. It is the #1 hospital on the East Coast, having been named #2 in America by U.S. News and World Report.

About ProTom International

ProTom International is a leading device manufacturer of proton therapy technology. We are steadfast in our mission to transform cancer treatment by expanding the accessibility of proton therapy and by developing proton tomography technology.

Combined with rapid return on investment and the precision of pencil beam scanning and the power of integrated imaging, ProTom's Radiance 330 is the choice for future proton therapy technology.