Elekta Beam Modulator gets 510(k) nod

Radiation therapy equipment developer Elekta has received U.S. Food and Drug Administration 510(k) marketing clearance for its Elekta Beam Modulator, a multileaf collimator designed for use with its medical linear accelerators.

The device shapes the radiation beam to more closely conform to the exact shape of the tumor, thereby allowing greater accuracy and smaller treatment fields, according to the Stockholm, Sweden-based firm.

By AuntMinnie.com staff writers
February 24, 2005

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